Viseven

DECEMBER 13, 2024

In the pre-digital era, clinical trials relied on traditional methodologies centered around in-person interactions and manual data collection, which presented numerous limitations. Data collection involved paper forms, diaries, and in-person interviews , which, while essential for documenting symptoms and outcomes, were prone to human error.

Health and Personal Care Stores 52

Health and Personal Care Stores Communication Documentation Pharmaceutical Companies 52

GMPSOP

FEBRUARY 10, 2024

Work, Health and Safety: The WH&S manager or specialist proposes and conducts a safety and environment training program that meets the WH&S and Environment compliance requirements as regulated by the local authorities. . – Archive the completed training into employee’s personal files.

Health and Personal Care Stores 52

Health and Personal Care Stores Documentation Packaging Compounding 52

GMPSOP

JULY 14, 2024

Quality planning for a pharmaceutical processing plant must be based on GMP guidelines provided by regulatory bodies, such as the FDA guidance (Food and Drug Administration), EMA guidelines (European Medicines Agency), and WHO (World Health Organization) guidelines for pharmaceuticals. Additional documents included each month.

Documentation 59

Documentation Customer Service Health and Personal Care Stores Communication 59