Insights into Clinical Research: Effective Strategies for Study Participant Recruitment & Retention In the world of clinical research, accelerated drug development can be a tedious process, taking over 10 years for medications to get to market. From bench to...
FIX-DOSED COMBINATION: APPROACHING AN OLD QUESTION WITH A NEW CONCEPT The development of generic fixed-dose combination (FDC) has seized increasing industry interest due to its advantages in disease management, patient compliance, and market benefits. For a generic...
FIX-DOSED COMBINATION: Global Development Strategy for Value Added Medicine The development of generic fixed-dose combination (FDC) has seized increasing industry interest due to its advantages in disease management, patient compliance, and market benefits. Adapting...
Pharmacokinetic Modelling Services for Drug Development Cost and time reduction are the core questions for all businesses to maximize their profits, regardless of their sizes, annual revenue, or business area. Especially, the high cost and long duration of the...
Clinical Trial Protocol Development: Bioequivalence-Generic Products A clinical trial protocol is the most important document that describes the objectives, design, methodology, statistical considerations, safety measures and organisation of a clinical trial. The...
Oncology Drug Development Formulation in Clinical Research Trials BPSI’s success story using normal healthy volunteers for Cost-efficient clinical development of a generic or improved formulation of oncology drug(s) Introduction Growing concerns about the high number...
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