Create a regulatory strategy

Our team will predict possible challenges and create a strategy to overcome them.


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Pre-screening of documents

Our experienced technical team audits each document for any errors, updations or information that is necessary for India’s updated norms.

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Quality and Compliances

API, Formulations, Co-ordination with Regulatory Agencies & final response to CAPA; GLP & GCP at Toxicity Centre(s) and CRO respectively.

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What About Us
About Us

BIOREG is an adjuvant for all your need to speed up your drug registration and approval process. Our experience, professional relations understanding, practicality and familiarity in the field of regulation of Drugs and Pharmaceuticals, Medical Devices, IVDs, Biologicals (Vaccines, Cell and Cellular therapeutics, Blood products, DNA, Biosimilars) products serve to ease your way through the process. BIOREG, is all with you to receive expert advice, 24 hour support, practical guidance and complete technical assistance right from the development stage to the commercial launch to the import and marketing in the Indian market.

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Our Services
Biologicals

Offering comprehensive regulatory solutions for biological products in India, ensuring compliance with CDSCO guidelines, clinical trial approvals, and post-market surveillance.

Drug

Complete lifecycle of the product. Leading regulatory services in India's pharmaceutical sector, guiding clients through CDSCO approvals, quality assessments, and post-authorization compliance.

Medical Device

Regulatory Guidance with our in-depth industry knowledge and strong track record.

Diagnostic Kit

Regulatory pathway development for the product.

Cosmetics

Nutraceuticals product registration services.

Food

Pathway for the Clinical development from Phase I to IV to help lifesaving treatments reach patients faster and thus leveraging the breadth of our clinical, regulatory, and therapeutic expertise.

CRO

Development of regulatory pathways for Drugs and Pharmaceuticals, Medical Devices, IVDs, Biologicals (Vaccines, Cell and Cellular therapeutics products, Gene therapeutic product, antisera ,Plasma derived products/Blood products, rDNA, Biosimilar, Cosmetics,)

Narcotics Regulatory Affairs

Clinical trials services including the Global clinical trials, preclinical studies, Testing of samples at central Drug Laboratory(CDL), Central Drug Testing laboratory (CDTL labs), National Institute of Biologicals(NIB).

Our Clients
Our Client Happy Say About Us