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ANDA: abbreviated new drug application; NDA: new drug application; BLA: biologics license application Legal Basis of ANDA, NDA, BLA Registration and R…
Pharmacovigilance is an important obligation for life sciences companies. Pharmacovigilance (PV), also known as drug safety, should be monitored throu…
Market access strategy is significant to win in the target market. A good market access strategy enables pharmaceutical companies to provide safe and …
DMF: Drug Master File; API: Active Pharmaceutical Ingredient Legal Basis Drug Administration Law of the People’s Republic of China (2019 Revision); Pr…
CTA: clinical trial application; BE study: bioequivalence study; MRCTS: multi-regional clinical trials Legal Basis Drug Administration Law of the Peop…
E-commerce market in China has become one of the most developed ones in the world, accordingly, the competition is fierce. Well-functioning ecosystem …
With its registered company in China, BaiPharm can be your trusted local authorized agent and provide support throughout the entire lifecycle of your …
To help companies evaluate their strategies for pharmaceutical regulatory management from the complex regulations and policies, clinical research, GMP…
To avoid delays in the review of product registration and to minimize the risk of rejection, it is critical for Chinese government officials to unders…
BaiPharm relies on its years in the pharmaceutical field and a reliable team of professionals experienced in international and Chinese regulatory affa…