Current trends in manufacturing for large volume parenteral in the pharmaceutical industry and future scopes
The current features of manufacturing of Large Volume Parenteral from receiving the API and excipient to the final dispatch of product addressed many features including, sampling errors, manufacturing errors other controls, and individuals involved in various phases. The pharmaceutical industry nowadays places a greater focus on production-related issues like handling manpower and quality-related problems and implementing systems like Good Manufacturing Practises, and other systems. To reduce reliance on humans and raise the quality of products, future trends and possibilities in automation in various areas like production, quality assurance, and quality controls were discussed in this paper. For the production of an enormous quantity of parentals, the roles and responsibilities of both the manufacturing team and the quality assurance team are crucial. Future manufacturing initiatives can reduce labour expenses while enhancing product quality, nevertheless, they will also encourage more automation research and development.
Authors
- Nilay Solanki (ORCID: https://orcid.org/0000-0003-1845-4740)
- Mehul Patel (ORCID: https://orcid.org/0000-0002-2304-3324)
- Tarang Patel (ORCID: https://orcid.org/0000-0002-0729-430X)
- Vatsal Patel (ORCID: https://orcid.org/0000-0002-3160-2907)
- Umang Shah (ORCID: https://orcid.org/0000-0001-6748-2137)
- Swayamprakash Patel (ORCID: https://orcid.org/0000-0002-6882-7042)
- Ashish A. Patel
Institutions
- Long Island University (US)
- Charotar University of Science and Technology (IN)
- Sardar Patel University (IN)
Publication Details
- Journal
- Prospects in Pharmaceutical Sciences
- Published
- 2025-02-03
- DOI
- https://doi.org/10.56782/pps.245
- Citations
- 1
- Primary Topic
- 3D Printing in Biomedical Research
- Type
- article
- Field-Weighted Citation Impact
- 0.67