Good Documentation Practices (GDP) & Technical Writing in Pharmaceuticals
Ensure data integrity and regulatory compliance through strong documentation practices and effective technical writing in pharmaceutical operations.
This training program provides comprehensive knowledge of Good Documentation Practices (GDP) and technical writing requirements within the pharmaceutical industry. It focuses on regulatory documentation standards, ALCOA+ data integrity principles, and structured technical writing for SOPs, batch records, validation documents, and quality reports. Participants will develop the skills necessary to produce clear, compliant, and inspection-ready documentation aligned with global regulatory expectations.
Course Content
Meet Your Instructor
Offered by Huksa, this L&D program is led by elite industry veterans—CXOs and Functional Heads with 25+ years of deep-domain expertise. You have the flexibility to customize the curriculum, select your preferred expert, and align the program to your organization’s specific objectives. Connect with the Huksa team to explore our array of top-tier trainers available for this course!
₹80,000.00
This course includes:
- Lessons 8
- Topics 32
- Duration 1 Day
- Quizzes 0
- Language English
Share
Report
