Nevisun Pharma offers a range of regulatory services to help clients in exploring the mind boggling scene of drug guidelines. Our experienced regulatory undertakings group is dedicated to ensuring that our products conform to every single relevant regulation and guidelines, both domestically and internationally.
Product Registration: We help clients in getting product registrations and endorsements from regulatory authorities, including the Drug Controller General of India (DCGI) and worldwide regulatory agencies.
Dossier Preparation: Our group gets ready thorough dossiers as per the Common Technical Document (CTD) design for accommodation to regulatory authorities.
Compliance Support: We provide ongoing support to ensure that our clients stay agreeable with all relevant regulatory requirements, including Good Manufacturing Practices (GMP) and Great Lab Practices (GLP).
Labeling and Packaging Compliance: We ensure that product marking and packaging comply with every regulatory requirement, including language and content necessities.
Advantages of Our Administrative Administrations:
Expertise: Our team of regulatory undertakings experts has broad experience with exploring regulatory requirements.
Efficiency: We smooth out the administrative interaction to speed up item enlistments and endorsements.
Compliance: We ensure that our clients stay consistent with all relevant regulations, reducing the risk of regulatory issues.
Market Access: Our regulatory services help clients with acquiring market access for their products, both locally and globally.
Peace of Mind: Clients can trust Nevisun Pharma to deal with all regulatory matters, allowing them to focus on their center business activities.
