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Precision Asia Pacific CRO Services
Driving clinical excellence in Asia Pacific, with Precision
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At Precision, we understand the intricacies of Asia Pacific's distinctive clinical research environment. In a region where each geography offers a unique clinical, regulatory, and cultural ecosystem, with Precision's Asia Pacific CRO services, you gain access to global expertise underpinned with regional insight to help you overcome barriers through every phase of your development journey.
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Harnessing the Asia Pacific advantage, with Precision
With our presence in Asia Pacific, we engage an expansive network of key opinion leaders, accomplished investigators, and premier research institutions. With Precision, your clinical studies in APAC will be guided by the best-in-class scientific and clinical researchers.
To further expand our Asia Pacific CRO services, Precision for Medicine acquired EganLee, an Australia-based firm with over 20 years of experience in clinical research across a wide variety of therapeutic areas, notably in oncology, neurology and hematology and with long-term relationships with numerous research sites.
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Precision Asia Pacific CRO services- Leading with regional expertise
Executing clinical trials in Asia Pacific requires adaptability and foresight. Precision's Asia Pacific team remains at the forefront of the constantly evolving regulatory and clinical research environment. Our clinical operations specialists, regulatory affairs experts, and experienced project managers bring vast experience in overseeing various clinical programs for both global and regional submissions.
With Precision's enduring partnerships in the region and exceptional delivery team, your trials in the Asia Pacific region are in capable hands.
8
Offices across Asia Pacific
250
Experts across multiple functions
3
Precision labs for integrated clinical development
The Precision team behind your success in Asia Pacific
Insights from Precision’s experts
Prepare for Asia Pacific’s regulatory and clinical development landscape with insights from Precision experts on current research, case studies and trends.
Case Study: Streamlining Radiopharmaceutical Clinical Trials
Navigating Site Activation Strategy Under the EU Clinical Trials Regulation
Considerations for Your Pre-IND Meeting With the FDA
Specialized capabilities in every stage of clinical development
Leverage an integrated infrastructure that reduces the inefficiencies inherent in complex development. Integrate lab and trial execution to increase speed to market. Incorporate manufacturing expertise for advances therapies to ensure scalability. Precision can customize and converge our capabilities for your program's unique needs.
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