I3cglobal.com Review

Based on looking at the website i3cglobal.com, it appears to be a company specializing in medical device regulatory consulting services for healthcare product manufacturers.

While the website highlights their expertise and commitment to compliance with EU, USA, and UK regulations, a thorough review reveals some areas that may warrant further consideration for those seeking comprehensive transparency and ethical business practices.

Here’s an overall review summary:

Company Focus: Medical device regulatory consulting, primarily for EU, USA, and UK markets.
Stated Experience: 23+ years of experience, 3400+ completed projects, 94% customer satisfaction.
Key Services: Regulatory documentation, registrations, technical consultation, data security, and cloud documentation.
Transparency of Pricing: Stated as “clear and consistent pricing on the website,” but actual pricing details are not readily accessible on the homepage.
Ethical Considerations: The core business of regulatory compliance is generally permissible, but the lack of immediate pricing information ands into customer testimonials or third-party verifications means a more cautious approach is warranted.
Overall Recommendation: Caution advised. While the service itself isn’t inherently problematic, the website’s structure and lack of direct financial transparency or detailed customer insights require a deeper look.

I3CGLOBAL positions itself as a “trustworthy company and sustainable partner” for navigating complex medical device regulations. They emphasize honesty, integrity, and fairness, claiming to have earned the trust and respect of existing customers. The site touts impressive metrics: “23+ Years of Experience,” “3400+ Completed Projects,” and “94% Customer Satisfaction.” They highlight their experienced technical consultants, fair pricing, on-time delivery, and robust data security with ISO 27001 certification and 24/7 uptime. However, while they state “clear and consistent pricing on the website,” actual pricing details or a clear pricing page are not immediately visible on the homepage, which can be a red flag for transparency. Furthermore, specific customer testimonials, case studies with verifiable outcomes, or external reviews from independent platforms are not prominently featured, making it difficult to fully gauge their customer satisfaction claims. For any business interaction, especially in a critical field like regulatory compliance, comprehensive transparency and readily verifiable credentials are paramount.

Here are some alternatives for ethical business consulting and compliance services:

PwC: A global professional services network, offering a wide range of consulting services, including risk assurance, regulatory compliance, and business transformation. They are known for their rigorous ethical standards and global reach.
Deloitte: Another one of the “Big Four” professional services firms, Deloitte provides audit, consulting, financial advisory, risk advisory, and tax services. Their regulatory and compliance services are extensive and adhere to high professional standards.
Ernst & Young EY: EY offers assurance, consulting, strategy, and tax services, including robust regulatory compliance consulting for various industries. They emphasize integrity and ethical conduct in their global operations.
Accenture: A leading global professional services company, Accenture offers strategy and consulting, interactive, technology, and operations services. Their compliance and risk management solutions are highly regarded, focusing on digital transformation and ethical practices.
IBM Consulting: IBM provides consulting services across various sectors, including regulatory compliance, data security, and digital transformation. Their long-standing reputation for technology and professional services makes them a reliable choice.
Booz Allen Hamilton: A major management and technology consulting firm, Booz Allen Hamilton works with government and commercial clients. They offer expertise in regulatory compliance, cybersecurity, and data management, with a strong focus on ethical frameworks.

Find detailed reviews on Trustpilot, Reddit, and BBB.org, for software products you can also check Producthunt.

IMPORTANT: We have not personally tested this company’s services. This review is based solely on information provided by the company on their website. For independent, verified user experiences, please refer to trusted sources such as Trustpilot, Reddit, and BBB.org.

Table of Contents

I3CGLOBAL.com Review & First Look

Based on an initial review of the i3cglobal.com website, it presents itself as a specialized consulting firm for medical device regulatory compliance.

The homepage immediately emphasizes their expertise in EU, USA, and UK regulations, positioning themselves as a crucial partner for healthcare product manufacturers worldwide.

The site is structured to convey professionalism and experience, highlighting their commitment to “honesty, integrity, and fairness.” This is a strong opening, aiming to build trust with potential clients who are navigating the complex and often stringent world of medical device approvals.

Initial Impressions of Professionalism

The website’s design is clean and functional, with a clear focus on the services offered.

Navigation seems straightforward, directing visitors to various regulatory areas such as EU MDR/IVDR, FDA 510k, and services related to drugs, food/food supplements, and cosmetics.

This organized presentation is crucial for a B2B service provider, as it helps potential clients quickly identify if their needs align with the company’s offerings.

The presence of contact information like an email address [email protected] and social media links though not explicitly visible in the provided text, usually expected under “Follow Us” adds to the professional façade.

Missing Key Information & Transparency Concerns

Despite the professional appearance, a critical examination reveals some significant gaps in transparency. While the site claims “clear and consistent pricing on the website,” there is no readily apparent pricing page or detailed service fee structure accessible directly from the homepage. This lack of upfront pricing information can be a major hurdle for potential clients who prefer transparent dealings and want to understand the financial commitment early on. In the consulting world, while custom quotes are common, a general range or a process for obtaining quotes is often outlined. The absence of this creates an immediate point of concern for ethical and straightforward business practices.

Verifying Claims of Experience and Satisfaction

The website boldly states “23+ Years of Experience,” “3400+ Completed Projects,” and “94% Customer Satisfaction.” While these statistics are impressive, the website does not provide verifiable third-party testimonials, case studies with client names even if anonymized to protect confidentiality, the context of success could be shared, or links to independent review platforms where these satisfaction rates can be corroborated. In a service industry where trust is paramount, particularly for regulatory compliance, having external validation of such claims is essential. Without it, these numbers remain self-proclaimed achievements that are difficult for an external party to verify.

I3CGLOBAL.com Features

I3CGLOBAL.com highlights several core features designed to attract medical device manufacturers seeking regulatory compliance assistance. Rishikeshyogaclub.com Review

These features primarily revolve around expertise, efficiency, and data security.

Understanding these proposed features is crucial for evaluating their service proposition, even with the aforementioned concerns about transparency.

Experienced Technical Consultants

Errors can lead to costly delays or rejection by regulatory authorities.

Fair Price & On-Time Delivery

I3CGLOBAL states that their “clear and consistent pricing on the website has attracted customers from around the world.” They assert that “People appreciate our commitment to fairness and reliability, making us a go-to choice for those who value transparent pricing with guarantee of quality.” The promise of “on-time delivery” is equally critical in a field where product launches and market entry depend heavily on meeting regulatory timelines. However, as noted, the lack of direct access to this “clear and consistent pricing” on the website remains a point of concern. While the commitment to fairness is commendable, the absence of actual price transparency undermines this claim for new potential clients.

Data Security & Cloud Documentation

One of the most appealing features, especially in the age of data breaches and strict privacy regulations, is their emphasis on “DATA SECURITY & CLOUD DOCUMENTATION.” They claim to be “Certified with ISO 27001 for data security,” which is a globally recognized standard for information security management systems.

This certification indicates a commitment to managing sensitive information securely.

They also mention “Operating around the clock with a 24/7 uptime guarantee” and diligently working to “maintain, and securely deliver documents via the cloud.” This commitment to data integrity and accessibility is vital for handling confidential regulatory submissions and intellectual property.

Secure cloud-based document management can streamline collaboration and ensure continuous access for clients.

Regulatory Documentation Services

The website explicitly lists a wide array of services crucial for regulatory compliance. For Medical Devices EU, they offer:

MDR/IVDR Technical Documentation or Technical File
Clinical Evaluation Report as per MDR article 61 and MEDDEV Rev 4
CE Marking for Standalone Medical Software
Appointment of European Authorised Representative for Non-European manufacturers
Appointment of UK Responsible Person UKRP for the UK market
Guidance on EU 2017/746 In Vitro Diagnostic Regulation IVDR

For Medical Device FDA, their services include: Soundasleepclub.com Review

510k Premarket Notification file development for Class I, II, and III Medical Devices
Cost-effective 510k documentation, US Agent, and FDA coordination services
FDA Medical Device Establishment Registration and listing along with UDI submission
Q Submission guidance for in-depth FDA feedback

They also extend services to DRUGS, including:

Guidance on 21 CFR 211 GMP
Drug Master File DMF assistance
US FDA drug establishment registration and product listing

And for FOOD/FOOD SUPPLEMENTS:

USA Bioterrorism Act compliance facility registration, prior notice
21 CFR 111 GMP compliance for manufacturing/packing human food supplements
FDA Label review for Food, Drugs, Cosmetics

Finally, for COSMETICS:

FDA Agents services
FDA Certificate assistance post facility registration
Voluntary Cosmetic Registration Program VCRP guidance, including ingredient statement filing

This comprehensive list of services suggests a deep understanding of various regulatory frameworks and a broad scope of operational capabilities.

I3CGLOBAL.com Cons

While I3CGLOBAL.com presents a strong facade of professionalism and expertise, a critical review reveals several significant shortcomings that should give potential clients pause.

These “cons” primarily revolve around transparency, verifiability, and the overall user experience for someone seeking to evaluate the company’s credibility.

Lack of Transparent Pricing

This is arguably the most significant drawback. Despite the website’s claim of “clear and consistent pricing on the website,” there is no dedicated pricing page or even a general indication of service costs. For a consulting service, while a custom quote is often necessary, the absence of any public information regarding pricing models, hourly rates, project fees, or a clear process for obtaining a quote immediately raises questions. This forces potential clients to engage in direct communication just to get basic financial information, which can be a deterrent for those performing initial research and comparison. Transparency in pricing is a cornerstone of ethical business practice, and its absence here undermines the company’s stated commitment to “fairness.”

Absence of Verifiable Customer Testimonials and Case Studies

The website prominently displays impressive statistics like “3400+ Completed Projects” and “94% Customer Satisfaction.” However, there are no specific customer testimonials, case studies, or client success stories that provide concrete examples of their work and its impact. There are no quotes from satisfied clients, no logos of companies they’ve assisted even if anonymized, and no detailed accounts of how they solved a client’s specific regulatory challenges. Without this independent validation, these statistics, while impressive, remain unsubstantiated claims. In a highly competitive and trust-dependent industry like regulatory consulting, third-party verification is crucial for building genuine client confidence.

Limited Public Information on Leadership and Team

The website mentions “experienced technical consultants” and “dedicated full-time experts,” but it lacks detailed profiles or bios of key team members, leadership, or even the general size and structure of their consulting team. Knowing who is behind the services, their specific qualifications, and their depth of experience can significantly influence a client’s decision. The anonymity of the consulting team makes it harder for potential clients to assess the specific expertise they would be relying on for critical regulatory submissions. This lack of transparency can be a red flag for companies seeking to establish long-term partnerships.

Insufficient Detail on Service Processes

While a broad range of services is listed, the website provides minimal detail on the actual process of engagement or how their services are delivered. For example, for “FDA 510k Premarket Notification,” while they mention developing the file, there’s no insight into the typical timeline, client involvement requirements, communication protocols, or specific methodologies. Understanding the workflow and what clients can expect during the engagement is vital for planning and setting realistic expectations. The general “READ MORE” links lead to more detailed service descriptions, but a high-level overview of their operational approach is absent from the homepage. Croccoprimainfanziashop.com Review

Over-Reliance on Self-Proclaimed Achievements

The website heavily relies on self-declared achievements “best in the industry,” “earned us the trust and respect” without providing external evidence.

While confidence in one’s services is good, these statements become less credible without supporting data from independent audits, industry awards, or widely recognized third-party rankings.

For a company dealing with regulations and compliance, a strong emphasis on verifiable, external validation would significantly enhance its perceived trustworthiness.

I3CGLOBAL.com Alternatives

Given the identified areas for improvement in transparency and verifiable claims on the i3cglobal.com website, it’s prudent for potential clients to explore established and highly transparent alternatives in the regulatory consulting space.

These alternatives often provide more readily available information about their methodologies, pricing, and client successes, fostering greater trust.

Reputable Consulting Firms with Regulatory Expertise

For comprehensive and verifiable regulatory consulting services, larger, well-established firms often offer a higher degree of transparency and a track record that is easier to verify through public information, client lists, and industry recognition.

PwC: PwC provides extensive regulatory consulting services for the medical device industry, covering everything from market access to compliance. Their global network and publicly available reports offer strong credibility.
Deloitte: Deloitte’s Life Sciences & Health Care practice offers deep expertise in medical device regulatory strategy, compliance, and quality management systems. They are known for their rigorous methodologies and adherence to global standards.
Ernst & Young EY: EY provides advisory services to medical technology companies, including regulatory compliance, digital transformation, and risk management. Their published insights and client testimonials provide a clear picture of their capabilities.
KPMG: KPMG offers regulatory and compliance services specifically tailored for medical device manufacturers, focusing on areas like quality systems, post-market surveillance, and global market access.

Specialized Regulatory Consulting Firms

Beyond the “Big Four,” there are many highly reputable specialized firms focusing solely on medical device regulatory affairs.

These firms often have deep niche expertise and can be excellent alternatives.

While some may not publish pricing publicly, their track records, leadership profiles, and client success stories are typically more accessible.

Emergo by UL: Emergo is a well-known global regulatory consulting firm acquired by UL. They specialize in medical device regulations, offering services across market access, quality management, clinical trials, and regulatory intelligence. Their extensive resources and global footprint make them a strong contender.
M Squared Associates: A highly respected medical device regulatory consulting firm that assists companies with FDA submissions, CE Marking, and quality system implementation. They often feature clear service descriptions and thought leadership.
RQM+: RQM+ is a leading medical device and diagnostics focused regulatory and quality consulting firm. They provide strategic regulatory planning, clinical, and quality solutions to help companies navigate complex global requirements.

When evaluating any consulting service, especially for critical regulatory matters, it is always recommended to: Oddsoncompetitions.com Review

Request detailed proposals: Including scope of work, timelines, and payment structures.
Ask for client references: And actually follow up with them.
Verify credentials: Confirm certifications, accreditations, and individual consultant qualifications.
Review engagement contracts: Carefully examine terms and conditions before committing.

How to Cancel i3cglobal.com Subscription

Given that i3cglobal.com is a business-to-business B2B consulting service, it is highly unlikely that they operate on a typical “subscription” model in the same way a software-as-a-service SaaS platform or a consumer media service would.

Consulting engagements are generally project-based or retainer-based, with specific contracts outlining the scope of work, deliverables, and payment terms.

Therefore, the concept of “cancelling a subscription” as one might for Netflix or a gym membership does not directly apply.

Understanding Consulting Engagements

For a company like I3CGLOBAL, clients typically enter into a service agreement or contract for specific regulatory consulting projects e.g., preparing a 510k submission, gaining CE Mark approval, or establishing a UK Responsible Person. These contracts would detail:

Scope of Work: The exact services to be provided.
Project Timeline: Expected start and completion dates, including milestones.
Payment Schedule: How and when fees will be paid e.g., upfront, milestones, monthly retainers.
Termination Clauses: Conditions under which either party can terminate the agreement.
Deliverables: What outputs the client will receive.

Process for Discontinuing Services

If a client wishes to discontinue services with I3CGLOBAL, or any similar consulting firm, the process would typically involve:

Reviewing the Existing Contract: The first and most crucial step is to carefully review the signed service agreement. This contract will outline the specific terms for termination, including notice periods, any penalties for early termination, and how intellectual property or deliverables will be handled.
Formal Written Notice: Clients should provide a formal written notice e.g., via email or certified mail to I3CGLOBAL, clearly stating their intent to terminate the engagement. This notice should adhere to any specific requirements outlined in the contract regarding the method and timing of notification.
Discussion and Handover: Following the notice, there would likely be a discussion to wrap up any ongoing work, transfer relevant documentation, and settle any outstanding payments for services rendered up to the termination date. Consultants typically ensure a smooth handover to the client or a new service provider.
Final Invoicing: I3CGLOBAL would issue a final invoice for any services completed or partially completed up to the termination date, in accordance with the contract terms.

Lack of Online Cancellation Option

Based on the typical business model for regulatory consulting firms and the information available on the i3cglobal.com homepage, there is no online portal, dedicated cancellation button, or self-service option for discontinuing services. All communications regarding contracts, project scope changes, or termination would occur directly between the client and I3CGLOBAL’s account or project management team.

Actionable Step: If you are a client of I3CGLOBAL and wish to terminate services, your immediate action should be to locate your service agreement and contact your assigned I3CGLOBAL representative to discuss the termination process as per your contract.

I3CGLOBAL.com Pricing

The I3CGLOBAL.com website explicitly states, “Our clear and consistent pricing on the website has attracted customers from around the world. People appreciate our commitment to fairness and reliability, making us a go-to choice for those who value transparent pricing with guarantee of quality.” However, a thorough examination of the publicly accessible pages, specifically the homepage content provided, reveals a complete absence of any visible pricing information, rate sheets, service packages, or even a direct link to a “Pricing” section.

Contradiction with Stated Transparency

This represents a significant contradiction between the company’s self-proclaimed commitment to “clear and consistent pricing” and the actual user experience on their website.

For potential clients, this lack of upfront pricing information can be a major barrier to entry and a point of concern regarding transparency. Mk2uk.com Review

Pricing Tiers: E.g., “Basic,” “Standard,” “Premium” packages for different service levels.
“Request a Quote” forms: Clearly signposted on a dedicated pricing page.
Average Project Costs: A general range for common service types.
Hourly Rates: Or daily rates for consulting time.

None of this appears to be present on the homepage, nor is there a clear navigation element pointing to such details.

Implications of Hidden Pricing

The practice of not displaying pricing can have several implications:

Lack of Immediate Comparison: Potential clients cannot quickly compare I3CGLOBAL’s costs with competitors, making their initial research more time-consuming and frustrating.
Forced Engagement: It compels interested parties to directly contact the company e.g., via [email protected] just to ascertain basic cost information. While this might be a lead generation strategy, it can also deter clients who prefer upfront transparency.
Perception of Exclusivity or High Cost: Some users might infer that the services are prohibitively expensive if pricing is not readily available, or that pricing is tailored on a case-by-case basis without a standard framework.
Reduced Trust: When a company claims “transparent pricing” but doesn’t deliver on that promise on its most visible platform, it can erode trust and raise questions about other claims.

How Pricing is Likely Handled

Given the nature of regulatory consulting, it is highly probable that I3CGLOBAL operates on a custom quotation model. This means that after an initial inquiry, they would likely assess the specific needs, scope, and complexity of a client’s project e.g., type of medical device, target market, current compliance status and then provide a tailored proposal with a detailed cost breakdown. This approach is common in complex consulting services, as projects can vary significantly in scope and required resources.

However, even with a custom quotation model, a company that truly values “transparent pricing” would typically:

State clearly on the website that pricing is custom and requires a consultation.
Provide an outline of their process for generating quotes.
Perhaps offer a general idea of the factors that influence project cost.

In conclusion, while I3CGLOBAL.com asserts transparent pricing, the current website content, particularly the homepage, fails to provide any actual pricing details, forcing potential clients into direct inquiry for even basic cost information. This represents a significant gap in their claimed transparency.

I3CGLOBAL.com vs. Competitors

When evaluating I3CGLOBAL.com against its competitors in the medical device regulatory consulting space, it’s essential to consider the various aspects that define a strong, trustworthy, and effective service provider.

Key differentiation points often include transparency, verifiable experience, breadth of services, and client support.

Transparency and Pricing

I3CGLOBAL.com: As established, I3CGLOBAL.com explicitly claims “clear and consistent pricing” but fails to display any actual pricing information on its public-facing website. This lack of transparency is a significant disadvantage.
Competitors e.g., Emergo by UL, RQM+, M Squared Associates: While many consulting firms also operate on a custom quote model, reputable competitors often provide more clarity on their process for obtaining quotes, offer educational resources about pricing factors, or sometimes even provide general service packages or fee structures for common services. They rarely make a direct claim of “clear and consistent pricing on the website” without backing it up visually. This makes it easier for potential clients to understand the general cost implications or the steps required to get a detailed estimate.

Verifiable Experience and Track Record

I3CGLOBAL.com: The website boasts “23+ Years of Experience,” “3400+ Completed Projects,” and “94% Customer Satisfaction.” However, these are self-proclaimed statistics without readily verifiable external testimonials, case studies, or client success stories. This lack of independent validation makes it difficult for potential clients to gauge the true extent of their expertise and client satisfaction.
Competitors: Leading firms like Emergo by UL, Deloitte, or PwC often feature extensive public portfolios, detailed case studies sometimes with client names or industry focus, and robust client testimonials on their websites. Many also have industry awards, recognitions, and thought leadership pieces published in reputable journals, providing verifiable proof of their experience and impact. For smaller, specialized firms, LinkedIn profiles of key consultants, or public speaking engagements can also serve as proxies for expertise.

Breadth and Depth of Services

I3CGLOBAL.com: The website lists a very comprehensive range of services covering EU MDR/IVDR, FDA 510k, drugs, food/food supplements, and cosmetics regulations. This broad scope indicates a wide range of capabilities across different regulated products and markets.
Competitors: Many competitors also offer broad services. However, their differentiation often lies in:
- Specialization: Some firms might be hyper-focused on, say, only EU MDR or only FDA submissions for a specific device class, offering deeper niche expertise.
- Integrated Solutions: Larger firms might offer integrated solutions that combine regulatory consulting with quality management system implementation, clinical trial support, or post-market surveillance.
- Global Reach: While I3CGLOBAL mentions EU, USA, and UK, global players like Emergo by UL have physical offices and local regulatory experts in numerous countries worldwide, offering a more truly global solution.

Data Security and Infrastructure

I3CGLOBAL.com: Highlights ISO 27001 certification for data security and 24/7 uptime for cloud documentation. This is a strong positive, as data integrity and security are paramount in regulatory affairs.
Competitors: Most reputable regulatory consulting firms place a high emphasis on data security. Many will also be ISO 27001 certified or adhere to equivalent robust security frameworks e.g., GDPR compliance, HIPAA compliance for US data. They might also highlight specific secure portals for document exchange or advanced encryption protocols. This is often a baseline expectation rather than a differentiator.

Overall Assessment

I3CGLOBAL.com presents itself as a capable regulatory consulting firm with a broad service offering. However, its significant shortcomings in transparency regarding pricing and the lack of verifiable external validation of its impressive claims put it at a disadvantage compared to many established competitors. Potential clients are forced to engage directly with I3CGLOBAL to gain basic information that more transparent firms readily provide. This can make the initial evaluation process more arduous and potentially raise concerns about the overall trustworthiness of the company. Competitors often excel in providing more accessible and verifiable information, which builds trust and facilitates a more straightforward client acquisition process.

FAQ

What is I3CGLOBAL.com?

I3CGLOBAL.com is a company specializing in medical device regulatory consulting services, assisting healthcare product manufacturers worldwide in achieving compliance with EU, USA, and UK regulations.

What services does I3CGLOBAL.com offer?

I3CGLOBAL.com offers a comprehensive range of services including regulatory documentation, technical file preparation MDR/IVDR, FDA 510k submissions, CE Marking for software, European Authorized Representative and UK Responsible Person appointments, as well as regulatory assistance for drugs, food/food supplements, and cosmetics. Sweethome3d.com Review

Does I3CGLOBAL.com have transparent pricing?

I3CGLOBAL.com states on its website that it has “clear and consistent pricing,” but a review of the publicly accessible homepage reveals no actual pricing information, rate sheets, or a dedicated pricing page.

Potential clients would need to contact the company directly for quotes.

How experienced is I3CGLOBAL.com?

According to its website, I3CGLOBAL.com has “23+ Years of Experience” in the industry, with “3400+ Completed Projects.” However, these claims are self-reported and not accompanied by third-party verifiable testimonials or case studies on the homepage.

Is I3CGLOBAL.com ISO 27001 certified?

Yes, I3CGLOBAL.com claims to be “Certified with ISO 27001 for data security,” indicating a commitment to information security management.

Does I3CGLOBAL.com offer on-time delivery?

Yes, I3CGLOBAL.com emphasizes its commitment to “on-time delivery” for projects, citing their experienced technical consultants and efficient processes.

How can I contact I3CGLOBAL.com?

You can contact I3CGLOBAL.com via the email address [email protected] or through their contact page linked on their website.

Does I3CGLOBAL.com provide services for FDA 510k submissions?

Yes, I3CGLOBAL.com states it provides services for FDA 510k Premarket Notification, including file development, US Agent services, FDA coordination, and Q Submission guidance.

Can I3CGLOBAL.com help with EU MDR/IVDR compliance?

Yes, I3CGLOBAL.com offers extensive services for EU MDR/IVDR compliance, including technical documentation, Clinical Evaluation Reports, and CE Marking for various medical devices and software.

What kind of data security does I3CGLOBAL.com offer?

I3CGLOBAL.com highlights its ISO 27001 certification for data security and mentions operating with a “24/7 uptime guarantee” for secure cloud documentation delivery.

Does I3CGLOBAL.com assist with food and food supplement regulations?

Yes, I3CGLOBAL.com provides assistance with FDA regulations for food and food supplements, including facility registration under the USA Bioterrorism Act, 21 CFR 111 GMP compliance, and FDA label review. Homedeco.lu Review

What is the customer satisfaction rate for I3CGLOBAL.com?

I3CGLOBAL.com states a “94% Customer Satisfaction” rate on its homepage, but this claim is not supported by external, verifiable testimonials or client reviews on the site.

Does I3CGLOBAL.com have an online cancellation option for services?

No, as a B2B consulting service, I3CGLOBAL.com likely operates on project-based contracts rather than subscriptions, so there is no online cancellation option.

Discontinuing services would typically involve reviewing your contract and communicating directly with their team.

Are there any customer testimonials on I3CGLOBAL.com’s website?

No, the provided homepage content does not include specific customer testimonials, case studies, or client success stories to substantiate their claims of high customer satisfaction.

Does I3CGLOBAL.com provide services for drug regulations?

Yes, I3CGLOBAL.com assists with drug regulations, including guidance on 21 CFR 211 GMP, Drug Master File DMF assistance, and US FDA drug establishment registration and product listing.

Can I3CGLOBAL.com help with cosmetic regulations?

Yes, I3CGLOBAL.com offers services for cosmetic regulations, such as FDA Agent services, FDA Certificate assistance, and guidance on the Voluntary Cosmetic Registration Program VCRP and ingredient statement filing.

What is the process for getting a quote from I3CGLOBAL.com?

While not explicitly stated on the homepage, based on the lack of public pricing, the process for getting a quote from I3CGLOBAL.com would likely involve contacting them directly via email [email protected] or their contact form to discuss your specific project needs.

Are I3CGLOBAL.com’s consultants full-time employees?

Yes, the website mentions having a team of “dedicated full-time experts” among their experienced technical consultants, suggesting a stable and committed workforce.

Does I3CGLOBAL.com focus on specific geographical regulations?

Yes, I3CGLOBAL.com explicitly states its specialization in delivering regulatory consulting services for compliance with EU, USA, and UK regulations.

How does I3CGLOBAL.com handle document delivery?

I3CGLOBAL.com states that it securely delivers documents via the cloud, operating around the clock with a 24/7 uptime guarantee, leveraging their ISO 27001 certification for data security. Antiskins.com Review