Who we are

CliniExperts is a leading pharma regulatory consulting firm based in Delhi, India. We specialize in providing regulatory affairs services for various sectors including Medical Device/IVD, Food Safety and Standards Authority of India (FSSAI), Drugs, and Biologicals. With a team of experienced professionals and a track record of successful regulatory support services, we are committed to helping our clients navigate the complex landscape of regulatory requirements in India.

What we Do

At CliniExperts, we offer a wide range of services to assist our clients with regulatory compliance in the Indian market. Whether you are an importer looking to obtain the necessary licenses and certifications for your products, or a manufacturer seeking authorization for manufacturing and selling your products in India, we have the expertise and resources to support you every step of the way.

Our services include but are not limited to:

• Biological Registration Certificate for Importers in India
• Import License for Medical Devices in India
• Import License For In-Vitro Diagnostic Kits in India
• Cosmetic Registration Certificate for Importers in India
• Test License to Import Medical Devices in India
• Biological Import License in India
• BIS Certification for Foreign Manufacturers in India
• Authorized Agent Support for Medical Devices, In-Vitro Diagnostics, Drugs, and Biologicals
• Test License to Manufacture Drugs and Medical Devices in India
• Permission to Manufacture Class B, C, and D Medical Devices
• Retention of Loan Manufacturing License for Class A and B Medical Devices
• Cosmetic Manufacturing License in India
• Compliance services for Food Supplements, Nutraceuticals, and Functional Foods
• Permission to Conduct Clinical Performance Evaluation for Drugs
• Wholesale Licenses for Drugs, Medical Devices, and Biologicals
• Non-Specified Product/Ingredient Approval for Functional Foods

Why you should use us

Choosing CliniExperts as your regulatory consulting partner means gaining access to a team of experts with in-depth knowledge of the regulatory landscape in India. We understand the complexities and nuances of the regulatory processes and requirements, and we work diligently to ensure that our clients meet all necessary guidelines and standards.

Our personalized approach to each client’s unique needs sets us apart from other consulting firms. We take the time to understand your specific requirements and tailor our services to meet your goals and objectives. With CliniExperts by your side, you can rest assured that your regulatory compliance needs are in capable hands.

What can you ask?

Visitors to our website or potential clients may have questions about our services, the regulatory processes in India, or how we can help them achieve their compliance goals. Here are some examples of questions you can ask us:

• What are the specific regulatory requirements for importing medical devices into India?
• How long does it typically take to obtain a cosmetic registration certificate for importers?
• Can you provide guidance on the documentation needed for obtaining a wholesale drug license in India?
• What is the process for obtaining BIS certification for foreign manufacturers?
• How can CliniExperts assist with compliance services for food supplements and nutraceuticals?
• Can you explain the steps involved in obtaining permission to conduct clinical performance evaluation for drugs?
• What sets CliniExperts apart from other regulatory consulting firms in India?

Feel free to reach out to us with any questions or inquiries you may have. Our team is here to provide you with the information and guidance you need to navigate the regulatory landscape in India successfully.