Life Science Consulting Services

Ensure Quality and Regulatory Requirements are Met Throughout the Product Lifecycle

PROPHARMA GROUP LIFE SCIENCE CONSULTING SERVICES

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 global, single source for expert insights pertaining to technical, quality compliance, and regulatory assistance throughout the product lifecycle, including:

Services Throughout the Product Lifecycle

COMMERCIALIZATION

These comprehensive services allow us to partner with clients who require large-scale manufacturing and postmarketing surveillance support.

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CLINICAL

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.

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Company Blog

January 15, 2020
Phase Appropriate Controls and GMPs in Cell and Gene Therapy
Compliance expert Benjamin Frey discusses the development of quality systems and controls for investigational… Read More
January 2, 2020
How to Safely Launch Medical Cannabis Products in Germany
Our expert's advice on how to navigate through the main challenges confronting you when… Read More
December 11, 2019
Five Steps Toward a Mature Data Integrity Culture
How can your company demonstrate the trustworthiness of GxP data as expected by regulators?… Read More
More Articles

UPCOMING Events

January 27, 2020
Pharmacovigilance and Risk Management Strategies Conference
DIA’s Pharmacovigilance and Risk Management Strategies Conference provides the foundation for strong str... Read More
February 18, 2020
SCOPE Summit 2020
Celebrating its 11th successful year, SCOPE Summit 2020 takes place February 18-21 in Orlando, FL. Over the co... Read More
March 23, 2020
DIA Medical Affairs and Scientific Communications Forum
DIA’s Medical Affairs and Scientific Communications Forum is designed for medical affairs professionals, b... Read More
All Events
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