WHO ARE WE?
Our comprehensive services including regulatory expertise, clinical trial support and market entry strategies are
designed to streamline your product from development to commercialization.
About Us
Pharma Peak Research (PPR) is a Philippine-based Contract Research Organization (CRO) focused on assisting emerging biotech companies without a local entity of operations in the Philippines in developing novel biopharmaceutical products.
PPR’s mission is to accelerate access to rapidly growing pharmaceutical and biotechnology markets by providing end to end services and holistic strategy.
Strategically, the PPR’s business model enables client to enhance product value by gaining strategic and regulatory alignment with Philippines. PPR also enables sponsors to efficiently and rapidly generate high quality clinical data to support registration of new biopharmaceutical products in the Philippines.
COMPANY MISSION
To accelerate access to rapidly growing pharmaceutical and biotechnology markets by providing end to end services and holistic strategy
Regulatory
Close coordination with stakeholders avoiding bottlenecks in review and approval process thereby fast-tracking timelines to initiate the trials
Operations
Ensures quality in the conduct of clinical trials and other trial related processes
Site
Selection of qualified sites and investigators with experience and good performance in their respective fields
PPR’s Strengths
*End-to-end Service with extensive experience in regulatory affairs, project management, and post-trial activities including registration and marketing
*Access to Pool of Experts including qualified investigators with good reputation and performance in their field
*Experienced and versed in conducting trials – Common and Rare Diseases
Therapeutics
We support clients in conducting Phase I-IV studies, Investigator Initiated Studies, across various therapeutic areas, including biologics, small molecules, bridging studies, and vaccines
Medical Device
We help conduct pilot, pivotal, and post-market surveillance studies for medical devices in various therapeutic areas.
Bioequivalence and
Bioavailability Studies
Helps sponsors enter local market by managing and implementing bioequivalence & bioavailability studies.
Epidemiological Studies
Support clients in conducting epidemiological studies to understand disease patterns, identify risk factors, and inform public health strategies
Non-interventional Studies
Gain real-world insights into therapies, understand disease occurrence, identify risk factors, and monitor long-term effectiveness across various therapeutic areas
Post-marketing Surveillance
Monitors safety, efficacy, and long-term outcomes after drug approval