MPC Pharmaceuticals is engaged in Contract Manufacturing of Finished Formulations in the form of Tablets, Capsules, Liquid Orals, and Sustained release preparations. The Company is equipped to manufacture “a wide range of pharmaceutical products in Solid & Liquid Dosage forms”.

MPC Pharmaceuticals aims to provide its customers with Novel Drug Delivery Systems and services including formulation development, Analytical method development and stability studies. The Tests are carried at par with highest standards of quality, reliability and compliance. MPC’s Success is the result of focusing on clients requirements at affordable cost & consistent quality. Customer Satisfaction / Service is on the priority list and it understands that the Association should result in its own growth and also the success of the clients. MPC Pharmaceuticals implements an unmatched global quality management system that is based on the desire to sustain a culture of operational excellence. Our company’s passion for quality goes way beyond business and statutory requirements.

MPC Pharmaceuticals has made strategic investments in common platforms of sustained release and combination product technologies, and in certain other key platforms to enhance drug delivery system capabilities. These technologies enhance the drug efficacy and safety by adopting a targeted therapy approach. The convenience of patients is an important factor while considering therapy solutions. The strategic aim is to formulate differentiated products that overcome the key challenges of conventional drug delivery systems and add value to existing products.

MPC Pharmaceuticals is committed to better healthcare for all, through quality products, achieved through manufacturing excellence, compliance to requirements and continual improvement in quality management system, for maximum customer satisfaction. Giving utmost importance to quality, MPC Pharmaceuticals has developed a sophisticated system and seamless procedure throughout the organization. This minimizes risk and enables us to produce superior quality products

QUALITY CONTROL

Quality control is an essential operation of the pharmaceutical industry. We have well experience qualified & competent dedicated technical persons in Various departments. Our QC department has all necessary instruments for analysis of API, finished products, packaging and related materials used. Quality Control refers to the features and characteristics of a product that bears on its ability to satisfy the needs of the consumer. Drugs must be marketed as safe and therapeutically active formulations whose performance is consistent and predictable.

Quality Assurance

Quality assurance department, a fully autonomous functionality is in place to keep track of each activity, parameters & processes to achieve the quality goal in totality. Quality of each medicinal product is assured by applying TQM techniques by the QA-Team. Quality assurance is a wide concept that covers all aspects that collectively or individually impact the quality of the product. That is, the sum of organized arrangements that are made with the aim of ensuring pharmaceutical products are of the required quality as per the intended use. Quality assurance is a good practice in the manufacture of pharmaceutical products, as it is the process of vouching for integrity of products to meet the standard for the proposed use. It is an obligation that ensures manufacturers meet the needs of end-user needs in terms of safety, quality, efficacy, strength, reliability and durability.

PROCESS OF THIRD PARTY MANUFACTURING

11. FINALIZING ORDER QUANTITY AND COMPOSITION.
Before starting the process of third party contract manufacturing, we have to finalize order quantity and composition of the product. While concluding the order quantity, we have to keep in mind minimum order quantities for the composition. For tablets and capsules, MOQ is usually between 50000 – 100000 units of Tab /Caps . While finalizing we have to check if the manufacturer has an approval for that composition
22. RAISING QUOTATION.
After finalizing composition and order quantities for contract manufacturing. We will raise a quotation which will include all the costs that you will incur. A quotation includes cost of product, packaging material, securities if any in case of smaller batches. It also includes any other charges that you would have to pay for the contract manufacturing process
33. REQUIRED DUCOMENTS.
To get a product made you need several documents. Some basic documents include Drug license and GST number. In some cases you will also require registration document of your firm or company. DL is issued by your local Food and Drug authorities. DL is of 2 types, one for retail and other for wholesale. GST number is issued by Government of India and is required for Third party manufacturing. In some cases some other documents like NON RESEMBLANCE CERTIFICATE and agreement for contract manufacturing are needed.
44. PACKING MATERIAL.
Promotional materials are used in every day sales by the medical representatives. Packing materials are the most proven marketing strategies. We always prefer best quality packing material by using all printing techniques.
55. PRODUCT MANUFACTURING.
There are certain quality standards set in GMP the production unit having the GMP certification, has to follow the guidelines set by GMP while manufacturing. GMP is a system that ensures the product is constantly produced and controlled according to the quality standards. GMP covers all the aspects of production from starting material to the hygienic staff. Every time products are made the correct procedure must be followed at each step
66. PRODUCT DELIVERY.
On-time delivery (OTD) is one of contract manufacturing’s most common measurements, On time delivery is a measure of process and supply chain efficiency which measures the amount of finish goods or services delivered to customers on time and in full. It helps determine how efficiently we are meeting our customer’s or agreed deadlines. It is an important priority to everyone in the business today.