BIOEQUIVALENCE
ABOUT
At Pro PG Pharma, we specialize in providing comprehensive project management services for Pharmaceutical Bioequivalence (BE) testing, specifically tailored to meet European regulatory requirements. As an extension of our wide-ranging offerings, this valuable service has emerged in direct response to the increasing demands expressed by our RLD/Comparator clients.
With our extensive expertise in the field, we are well-equipped to oversee and guide the entire BE testing process, ensuring compliance, efficiency, and optimal results for our clients. As your trusted partner, we understand the complexities of the regulatory landscape and industry standards, allowing us to navigate the intricacies of BE testing on your behalf.
WHY US?
Pro PG Pharma is able to run the BioEquivalency Testing in North America and provide the monitoring required for EU, USFDA, TGA and MHRA standards.
OUR SERVICES
Our services encompass all aspects of project management, from designing study protocols and selecting suitable comparators to managing timelines and resources. We coordinate closely with top-tier testing facilities, monitor data collection and analysis, and ensure that your BE testing adheres to stringent regulatory guidelines.
By entrusting your pharmaceutical development project to us, you can alleviate the burden and focus on other critical aspects of your endeavor. Our commitment to compliance, efficiency, and delivering exceptional results underscores our dedication to providing high-quality services tailored to meet your specific needs.
WE LOOK FORWARD TO WORKING WITH YOU
Choose Pro PG Pharma as your partner in pharmaceutical development services. Together, we can navigate the complexities of BE testing, meet regulatory requirements, and drive the success of your projects.