Regulatory agencies demand that manufacturers maintain compliance throughout all stages of a product’s lifecycle, from concept to commercialization, including postmarket compliance. Maintaining compliance for your particular product at its current status in the lifecycle is a complex challenge unique to each company, and one which requires continuous attention and support.
ProPharma Group specializes in solving these complex challenges. As an extension of your team, we care about not only the progression of your products, but furthermore the safety of your products and the patients who use them. Our highly trained professionals seamlessly integrate with your organization to do more than simply identify potential risks. We provide recommendations to mitigate those risks, work side-by-side with you to implement improvement plans, and train your staff how to address those risks when our job is done.
ProPharma Group is your single source for expert insights pertaining to technical, quality compliance, and regulatory assistance throughout the product lifecycle, including:
These comprehensive services allow us to partner with clients who require large-scale manufacturing and postmarketing surveillance support.View Services
Whether you are in Phase I, Phase II, or Phase III, ProPharma Group has wide breadth of services catered to your unique, product development and pre-approval scale up needs.View Services