It can be tough sledding out there for challenger pharma brands. Attempting to make inroads in saturated markets against established incumbents is difficult — no matter how bespoke or effective the ...

Researchers engaged in pharma research and development must adhere to current Good Laboratory Practice (cGLP) and Good Manufacturing Practice (cGMP) standard operating procedures. Such regulatory ...

In a time when COAs are more nuanced, critical and complex than ever, researchers can turn to best practices to move forward ...

ASCs strive to offer a quality of care and operate at a level of excellence that at least meets the standards set by hospitals, and ASCs are often successful are exceeding these standards. But one ...

Residues of pharmaceutical products can enter the environment during the manufacturing process, during usage, and disposal. With the growing trend in sustainable practices, the translation of ...

Strengthen information governance with clear policies for data classification, retention, and legal holds to meet industry regulations and ensure defensibility. Embed compliance and collaboration ...

The vast majority of drugmakers are either considering or have already established direct-to-patient (DTP) programs, cutting out middlemen to offer services like virtual care consultations, payment ...