Clinical Expertise in Asia Pacific
Medpace is a global CRO, with a local presence in Asia Pacific
Medpace is a global CRO, with a local presence in Asia Pacific
Asia Pacific Drug Development Services
As a global CRO with an operational footprint across 40 countries, Medpace has broad experience designing and conducting Phase I-IV clinical trials around the world. Our medical, regulatory, and operational experts have the resources to advance your medical therapeutic in any region. Since establishing our Asia Pacific (AP) presence in 2004, our medical and operational specialists have country-specific expertise, which allows them to integrate local language, culture, and requirements into study conduct, to deliver faster enrollment, and obtain access to country-specific patient populations. Our regulatory experts can plan and coordinate each aspect of regulatory strategy and engagement — locally and globally.
Do you have an upcoming clinical trial that requires seamless execution amid the complex landscape of global development? Fill out our brief form below to learn more about how Medpace experts can help you design and conduct your study anywhere in the world.
Medpace at a Glance
We’re operational around the world – wherever research is happening.
Full-Service Approach to Global Clinical Research
Our AP based medical, operational and regulatory experts are available to discuss the challenges, timing and requirements for your upcoming clinical development. We can coordinate with our cross-functional teams around the globe to set your trial up for success.
The Medpace Advantage:
- A specialized physician team with extensive clinical experience
- Well-profiled networks of sites across multiple therapeutic areas (including oncology, advanced therapies, and CNS)
- Comprehensive regulatory affairs and operational experts who work collaboratively with our medical team
- Fully integrated laboratory services and an imaging core lab to seamlessly support your study
- Early phase study services and our state-of-the-art Phase I Unit facility
Medpace has the global reach to plan and execute your clinical development plus the local expertise to manage the nuances of each country. Our size and our operating model ensure you will get the attention and priority you need.
Medpace is Trusted by Biotech®
Biotechs are confronted with an ever-changing slate of top priorities. The ability to fully rely on your CRO to execute studies – almost independently – allows you to focus on other pressing issues.
There’s a reason 90% of our clients are small to mid-sized biopharma companies. Being Trusted by Biotech® means that we form collaborative relationships and our teams are as invested in the science of your products as much as you are. At the same time, we are large enough to conduct complex trials globally, yet small enough to maintain a higher level of commitment.
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Request for Information
If you are a drug or medical device sponsor, please fill out this Request for Information Form and a Medpace representative will be in touch with you shortly.
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