Different Types of Quality Control in Pharmaceutical Industry

Quality is one of the crucial aspects on which the pharma products are evaluated for their quality and efficacy. It should be non-negotiable for the companies such that it not only boosts their market value, but also gives end-users the desired results. Regulatory bodies are also imposing strict quality control guidelines, ensuring the overall safety of the drugs.

The in-depth research and analysis, combined with high-quality content, not only benefit pharmaceutical companies but also yield impactful outcomes for their clients. These days, people are getting very aware of the innovative and effective medications. Thus, safeguarding the quality also becomes very important.

For the entrepreneurs who are seeking a reliable company to partner with, whose products meet all the quality standards, and provide a stable platform to grow is none other than Adorefem. We are recognized as a top gynecology pharma company in India with a wide range of ISO-GMP-certified products.

In this blog, we will highlight all the kinds of quality control that are necessary to be maintained in any pharma company. In addition, you will also gain insights into how partnering with us could be a credible business move.

Different Types of Quality Control in the Pharmaceutical Industry

Well, the term quality control might seem simple, but it is ensured via several steps, such as documentation, rigorous testing, and most importantly, regulatory compliance. So, here will discuss the series of mandatory checkpoints to be followed closely at any cost:

Raw Material Quality Control

The sourced material which are going to be the foundation of any medication should be thoroughly checked and analysed. A company should choose a reputable company for the raw material, and do its laboratory testing, safeguarding the purity and safety. Prepare a documentation review such that whenever an authority needs the proof, you have it.

A company should assign a different team and provide given with proper knowledge about how to handle and store them. It will prevent them from any contamination, and long-term durability will be maintained. Lastly, follow the guidelines set by GMP, which includes ICH Q7, for Active Pharmaceutical Ingredients (APIs).

In-Process Quality Control

As soon as the formulation of the medication starts, do proper monitoring at each stage to know whether the process is proceeding as per the guidelines set by the WHO or not. Do not forget to do the in-between testing of the drugs, which includes

• Hardness,
• Weight variation
• Physical appearance, etc.

This will help in the early detection of errors, aiding in smoothing production and thus enhancing the overall productivity of the products.

Finished Product Quality Control

This is the process in which the final testing of the product will be done after the manufacturing process is finished. Check whether the product is meeting the specialized needs for which it was formulated, such as testing for its purity, stability, and sterility. Also, analyze how the product is reacting with environmental factors such as moisture, humidity, and temperature. This will help you understand its storage conditions and shelf life.

Microbiological Quality Control

This is a phase in which it has been tested that the product is free from any harmful microorganisms, which might contaminate or affect the overall quality of the product. Pathogen-specific assessments and sterility testing are done to determine whether there are any loopholes. Proper environmental conditions are also maintained so that no external factors can hamper the quality of the products.

Packaging Material Quality Control

In this stage, proper analysis is done to choose a durable packaging material for the medication being formulated. It includes many components such as bottles, blisters, caps, labels, and foils that are safe, non-reactive, and compliant with product standards. This safeguards not only the quality but also ensures that the products have a good shelf life.

Documentation Review and Reporting

All the documentation done during the production and packaging of the products will be reviewed by the Quality control personnel. This will help in analyzing the reports to ensure that they meet the ISO-GMP standards thoroughly. Lastly, there comes the releasing, rejecting, and reporting stage. In case any error is found, then the review will be rejected; however, if all went right, the documentation will be sent to higher regulatory authorities for approval.

Partner with Adorefem for Reliable, Quality-Driven Pharma Products

Adorefem, an experienced company with specialization in gynae products, ensures to follow all the quality standards. They have distinct teams for each stage that closely monitor each stage and come up with the medication that stands strong with the WHO-GMP guidelines. Our well-experienced staff and excellent R&D support in a smooth manufacturing process. We have a wide range of products that address almost every concern that women go through in their lifetime. It includes heavy menstrual bleeding, early menopause, infertility, etc.

We have the entire set of quality documentation, along with the regulatory compliance approval. Thus, if you are looking to jump into the pharma sector with a commendable company for whom quality and efficacy are non-negotiable, then Adorefem’s doors are open for you.

Address: SCO No. 3, Cheema Complex, Chandigarh-Ambala Highway, Zirakpur, Punjab, India-140603

Email: adorefemmailbox@gmail.com

Phone Number: +91-9877530744, +91-9417466020