• Devkar Nilesh Balkrishna
• Dama Ganesh Yogiraj
• Joshi Sumit Ashok
• Gaikwad Asmita Vikas

Good Documentation Practice (GDP) is an integral part of good manufacturing practices Ensuring the integrity of data collection and reporting is imperative for supporting the development, registration, commercialization, and life-cycle management of pharmaceutical products. Documents serve as a mirror, reflecting the true image of any pharmaceutical industry. Various measures, both collective and individual, are in place to guarantee that documentation, whether in paper or electronic form, is attributable, legible, traceable, permanent, contemporaneously recorded, original, and accurate. This commitment to robust documentation practices not only meets regulatory requirements but also establishes a foundation for transparency and reliability throughout the pharmaceutical lifecycle.

Document, Compliance, Alcoa +, Quality, Data, Integrity.

"GOOD DOCUMENTATION PRACTICES ", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.11, Issue 6, page no.f244-f252, June-2024, Available :http://www.jetir.org/papers/JETIR2406527.pdf

"GOOD DOCUMENTATION PRACTICES ", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.11, Issue 6, page no. ppf244-f252, June-2024, Available at : http://www.jetir.org/papers/JETIR2406527.pdf