Compliance is the best medicine
Finest quality pharmaceutical products for Worldwide Markets!
To manufacture products that are consumed by patients across the world requires stringent standards and consistent quality assurance.
We believe it's a challenge to be a manufacturer of finished pharmaceutical formulations that will be truly world class. In our quest for perfection, we have left no stone unturned right from the selection of the finest raw material, using state-of-the-art technology and processes to bringing out the finished formulations. Helping us produce the finest quality pharmaceutical products. Frequent quality parameter checks are conducted to ensure a perfect product. Quality Control Lab plays a vital role in regulating the quality of products.
We take our role as a global manufacturer/supplier of finished pharmaceutical formulations very seriously and surpass any standards set by worldwide regulatory authorities. All our products are manufactured as per the regulations and guidelines of the WHO under Good Manufacturing Practice . We implement this through our global quality management system, that is based on planning, implementation and control with independent controls that guarantee safety and reliability, ensuring that only the finest quality pharmaceutical products roll out of our facility.
The Regulatory Affairs department is an important part of the organizational structure of pharmaceutical companies. Internally it liaises at the inter phase of drug development, manufacturing, marketing and clinical research. Externally it is the key interface between the company and the regulatory authorities.
In Placidus, Regulatory Affairs professionals play an important operational role by considering the best processes to follow and enabling structured interaction with regulatory authorities.
Our regulatory team ensures that the information and data to be conveyed and discussed with the regulatory bodies are presented in the right way and form. They develop the regulatory strategy, prepare and compile the questions and briefing documents.