Quality audits specifically examine how well product designs and processes meet specified standards and regulatory compliances. They are performed periodically by internal people
In the ever-evolving landscape of regulated industries such as life sciences, pharmaceutical manufacturing, gene therapy and medical devices; the demand for cutting-edge technology
Clinical trials are crucial for advancing medical research, but ensuring their integrity and adherence to ethical guidelines is paramount. Good Clinical Practice (GCP)
The complexities of quality improvement within the pharmaceutical realm present a tough challenge. As the healthcare landscape evolves, aligning industry shifts across diverse
Maintaining strict quality standards, efficient processes, and compliance with regulatory requirements is paramount in the highly regulated and complex pharmaceutical industry. Document control
Data integrity reaffirms the pharmaceutical industry’s commitment to manufacturing safe, effective drugs that satisfy quality standards. Simultaneously, data integrity is a vital tool
This article provides a clear insight into the significance of data integrity within the framework of current good manufacturing practice (CGMP) for pharmaceuticals,
As manufacturers in the pharmaceutical industry face new-market demands, intricate supply chains, and evolving regulations, there is a growing need to reassess outdated
In a recent announcement, Health Minister Mansukh Mandaviya emphasized the importance of complying with Schedule M of the Drugs and Cosmetics Act, prepared
The pharmaceutical industry is critical in safeguarding public health by researching, developing, and manufacturing life-saving drugs. However, this sector operates in a highly