Clinical and Medical Affairs

The Karya Clinical and Medical Affairs membership offers extensive experience across all trial phases, providing innovative solutions to efficiently bring products to market.

With decades of industry expertise, they stay current with evolving regulations.

Clinical Operations Services

Clinical operations are vital in executing clinical research, covering Phase I to IV trials.

With trials becoming more complex due to stricter regulations, some organizations choose to outsource to Contract Research Organizations (CROs) for end-to-end trial support. The Karya marketplace platform's clinical operations members collaborate to optimize trial design, implement patient-centric approaches, and provide guidance throughout the development lifecycle.

Global Clinical Trial Management Teams

Offering local expertise with a global reach, the Karya platform provides flexible teams to meet trial needs across regions.

Their experienced teams streamline multi-region studies with confidence and agility.

Medical Monitoring Services

Medical monitoring consultants from the Karya platform ensure safety and compliance throughout trials, from pre-trial planning to end-of-trial review.

They assist in meeting quality and compliance requirements across various therapeutic areas.

Clinical Trials

For Pharmaceuticals, Biologics, Medical Devices, and Diagnostics.

The Karya platform supports trials across all phases and therapeutic areas, maintaining expertise in cutting-edge technologies and repurposing products

Study Phases and Therapeutic Areas

Karya provides deep expertise across pharmaceutical, biotechnology, medical device, and diagnostic industries.

The Karya marketplace platform membership anticipates obstacles and develops tailored strategies for clients' unique needs.

Global Medical Writing Transparency

The Karya platform provides scalable medical writing solutions across clinical, nonclinical, device, and diagnostics areas.

Their global team of medical writers ensures quality and collaboration in delivering documents for clinical trials.