Company Profile

Primus Pharmaceuticals is a young and novel dynamic drug delivery systems (NDDS) company in India that provides a range of effective solutions to optimize the delivery of pharmaceutical products.

Primus Pharmaceuticals  was established by Mr. Suresh Kumar Dua early 2010  located in India. Driven by the vision to provide the best possible, range of international quality products at competitive prices through integration, research, innovation, technology & development.

We have a world class oral solid dosage form manufacturing facility for Pellets, Micro-Pellets and Granules approved by regulatory authorities of developed countries.

We want to carve out a niche in the field of Novel Drug Delivery System(NDDS) & would like to be known as one of the Leading Global Research Based, Drug Delivery Companies, with an expertise in novel drug delivery systems, constantly strive towards building and strengthening upon our intellectual property.

Today, Primus Pharamceutical is dedicated to achieving the highest levels of quality in everything we do to measure up to the high standard set by the customer, local & overseas customers, every time. We deliver the products as per the set schedules with excellent quality at a very competitive price. With this dedication towards quality, we are able to provide world class products. Our strength lies in our ability to provide a tailored solution to fulfill the specific needs of its customers in question.

Our current activities include manufacturing of pre-finished and finished formulations
Primus Pharmaceutical is managed by an experienced Board of Directors, who are assisted by a team of dedicated and qualified professionals drawn from various disciplines.

We are thankful to all our customers, agents, employees and well wishers for their continuous support to convert our ideas into technology and technologies to success and profit.

We welcome customers from worldwide to start a promising business relationship with us!


Our Team:

We believe that strength of any successful organization rests in its people, and the people create the heart of the organization. We respect the individual and strive to maximize the operational freedom of each employee.

Employees work in modern environments, which facilitate and encourage learning, participation and out of the box thinking. The corporate culture at Primus is strongly influenced by team-spirit which weaves all the employees together towards a common goal.

There are about 50 employees engaged in various divisions in this unit.

The division-wise employees number is given below

PRODUCTION : 05

QUALITY CONTROL : 06

QUALITY ASSURANCE : 03

STORAGE & DISTRIBUTION : 04

SERVICES : 05

WORKMEN : 27

 

Quality Management is being practiced at M/s Primus Pharmaceuticals under the following three heads.

Control Function: The Control function looks after the approval of Raw Materials,Packing materials, Finished products, and inspection of In-process materials with proper documentation.

Technical Function: Q.A’s Chief Technical support activities include:

  • CGMP / CGLP Training.
  • Review and approval of Specifications
  • Documentation Controls
  • (I.e. Sops, Master records, Batch records, Validation&Calibration records)
  • Support to process / product validation
  • Conducting Self-Inspection /Internal Audits & Compliance Audits.
  • Calibration of Instruments/ Equipments
  • Compliance Function: This relates to Quality Assurance Controls that are exercised on Vendor Control, Product release etc. Q.A. In charge is responsible for all the Quality Management Functions of the Unit. He is assisted by a team of Scientific personnel who are adequately qualified and experienced to certify quality of drugs. Senior technical personnel are qualified from recognized academic institutions and are also approved by Local Drug Control Authorities as a mark of recognition of their expertise.

     

    Q.A. In-charge reports to the Proprietor of the firm both on day to day administration matters and technical matters.

    Q.A. In-charge is vested with Authority to approve or reject all incoming Raw/Packing materials, in-process materials and her/his team has the authority to review production records. This is to ensure that no errors could occur, if they occur, they have been fully investigated.

     

    • Quality Assurance team is responsible for approving or rejecting all specifications and procedures that have impact on the quality of the finished products.

     

    As a matter of practice, all documents concerning the products, prepared specifications and Standard Operating Procedures are sent to

    Q.A. In-charge for Approval. Training is imparted to all technical personnel at the entry level. In addition, periodic refresher courses are given. By this process, each person is assured to possess the required competency for discharging his / her assigned duties and responsibilities effectively.

    •  

    • Quality Assurance team is responsible for approving or rejecting all specifications and procedures that have impact on the quality of the finished products. As a matter of practice, all documents concerning the products, prepared specifications and Standard Operating Procedures are sent to

    • Q.A. In-charge for Approval. Training is imparted to all technical personnel at the entry level. In addition, periodic refresher courses are given. By this process, each person is assured to possess the required competency for discharging his / her assigned duties and responsibilities effectively.


    • Vendors premises ( indigenous ) are inspected by Quality Assurance personnel periodically, in addition to the testing and release of procedures of all input materials. Such inspections are necessary to get confidence on the quality systems being followed at Vendor’s premises. Spot Audits of problem areas are conducted within the departments basing on necessity in addition to the periodic GMP audits of different departments.