0 reviews
Pharmadesk specializes in consulting and full project management services tailored for generic pharmaceutical companies, focusing on Bioequivalence (BE) studies and related activities. We support companies throughout the entire process—from product feasibility assessments and selecting the right CRO, to medical writing, project management, study monitoring, analysis of failed BE studies, IVIVC, and regulatory support for BE submissions. What sets us apart is our highly skilled, technically proficient team that consistently delivers projects on time. We offer valuable insights into your generic product development and implement risk mitigation strategies for your bioequivalence programs, helping save your organization significant costs. Our team of over 25 experienced professionals—including project managers, clinicians, pharmacologists, formulators, QA specialists, regulatory and analytical experts, along with an ex-MHRA consultant—takes full ownership of your BE studies. We carefully evaluate and select CROs in India to ensure your studies are completed efficiently and successfully. Having managed more than 380 successful BE studies submitted to EU and USFDA authorities, and with extensive experience across multiple products and markets, we’ve developed well-defined processes for every step of the BE study cycle. Plus, we assign a dedicated project manager to each project, ensuring personalized attention and smooth execution from start to finish.
Poor
0 reviews
There are not enough reviews yet to generate a summary. Be the first to share your experience and help others choose with confidence.
You can write your full review now. We will ask you to login/signup, and publish after email verification.
No reviews yet. Be the first to leave one.
No photos yet.