Rigorous project management is the driving force at Bioeq that helps us meet customer deadlines. The average time to file a DMF at Bioeqcare being 8 months and average time for a dossier development being 8 months, stand as testimonies to this fact.
Service Offerings:
Co-development
When it comes to innovation, Bioeq understands the power of combining resources to achieve goals with maximum efficiency. This enables our research and development team to offer co-development of novel molecules for pharmaceutical advancement.
Custom Synthesis
We provide custom synthesis of drugs as per customers’ requirements. This is done so with precision and caution. With over 1,100 quality experts and several monitoring laboratories, inconsistencies (if any) are checked for, thereby ensuring quality and timely deliverables. We also offer flexible and feasible cost options.
Dossier development services
We like to be thorough with our production and manufacturing process by focusing on:
- Product information
- Clinical and manufacturing applications and requirements
- Scientific reports
- Regulatory dossiers
More importantly, when it comes to drug development, we provide dossier services with the same diligence.
Our ever-growing portfolio
We are extremely grateful for the wonderful family of clients and customers that we have built across the globe.
API's
FDFs
ANDAs
DMFs
CEPs
DOSSIERs