At Pharmacy Innovations, we actively participate in clinical trials to advance medical knowledge and improve treatment options. By collaborating with researchers and healthcare professionals, we help develop new medication formulations tailored to specific patient populations, such as children or individuals with allergies.
Our involvement in clinical trials allows us to customize doses, explore alternative delivery methods (such as liquids or creams), and create unique medication combinations that are not available in standard forms. This enables us to fill treatment gaps where traditional medications fall short, offering potential solutions for conditions that are difficult to treat with commercial products.
Additionally, we ensure that compounded medications are prepared in the most effective, patient-friendly forms, enhancing treatment adherence and improving overall health outcomes.
Pharmacy Innovations specializes in high-quality compounding for clinical trials, adhering to the highest industry standards.
As a 503A sterile and non-sterile compounding pharmacy lab, Pharmacy Innovations is USP 795, USP 797, and USP 800 compliant for both sterile and non-sterile compounding.
Our compounding laboratories are designed to enhance our capabilities in working with clinical trials.
Our Pharmacy Management Team is trained in Good Clinical Practice (GCP), ensuring compliance with regulatory standards for clinical trials in the U.S. and internationally.
Good Clinical Practice (GCP) Certifications
With over 300 years of combined experience, our team includes skilled pharmacists, researchers, clinical coordinators, and regulatory experts dedicated to clinical trial success.
Sterile & Non-sterile compounding
Customization and variation
Blinded or unblinded product options
Commercial products available with investigator and subject blinding
Over 30 years of experience with clinical trials
During the initial research phase, we collaborate with pharmaceutical companies, universities, and other institutions to ensure the stability, delivery method, concentration, dosage, pH, packaging, labeling, quality, and accuracy of investigational drugs before advancing to clinical trials. This process may involve developing new drugs or optimizing existing formulations with improved combinations or dosing strategies.
We maintain consistent quality control across international trials, ensuring compliance with protocols and regulations while upholding our pharmacy’s reputation and the validity of trial results. Robust monitoring mechanisms are in place to guarantee adherence to industry standards.
As our pharmacy gains experience from compounding for international trials, we continue to refine our processes and share knowledge across our organization. We regularly update the team’s understanding of international regulations and best practices through training and professional development.
After completing international trials, we gather feedback and insights to improve future endeavors. We have incorporated lessons learned into future trial planning and execution.
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