Pharmi Med Ltd is an experienced validation company
that offers the full spectrum of compliance services
for the Pharmaceutical, Biotech and Medical Equipment industries.
Our experts have prepared an infographic guide pack for your regulatory and compliance journey, including development of new products, getting your medical device to market, continual improvement of the Quality Management System, the new MDR, Risk management for medical devices as well as return on investment.
CLICK THE BUTTON BELOW TO GET YOUR GUIDE PACK TODAY!
My time at Pharmi Med has been a very rewarding experience. This unique opportunity gave me an insight into the medical device industry and helped me decide my career path. I became familiar with international standards, such as ISO 13485, while developing my skills in technical writing and risk management activities. Adnan is a also great mentor who continuously encouraged me and gave me opportunities to attend events such as the Med Tech Innovation Expo in Coventry and the Medilink Pitching event. Choosing to work with Pharmi Med has certainly been one of my best decisions!
Working at Pharmi Med has been one of my best employment experiences. During my time there, I had the opportunity of gaining experience in validation and verification, risk management, design development and control plans, failure analysis and occurrence analysis. I also gained valuable insight into medical device regulation, regulatory bodies and relevant international standards. Adnan was a fantastic mentor, providing support and encouragement, which made working part time and studying simultaneously more than manageable. Working at Pharmi Med ultimately helped me choose my career path!
We extensively worked with Adnan on a major supplier transition project for ConvaTec, to our Company GA2 Medical Sdn Bhd. This involved advising on validations, risk management activities and protocol and report preparations. Throughout, Adnan’s approach was systematic, adaptable and professional and his technical knowledge of the regulatory requirements, and what that specifically meant for us and our internal procedures and activities, was very impressive. He always made himself available for discussions and advice which made the process of change and implementation straight forward for us, in a not-so straight forward, and often demanding, situation.
In a challenging and changing medical device environment, you need the right people in your corner. Based on our experiences, we would strongly recommend Adnan as your Quality, Regulatory and Validation Consultant. He will be in your corner.
Adnan performed auditing of our company QMS. He was methodical and detail-oriented. His feedback and findings were useful in improving our QMS structure and implementation. He is an experienced quality management professional with genuine desire to add value. We will recommend his services to organisations needing quality and regulatory input. OPSL.
Adnan recently supported us on our ISO13485 2016 transition through extensive gap analysis and appropriate updates to our QMS, which lead to a successful transition, he supported us as an Interim Quality Manager as well as our regulatory work. In addition he and his team have been involved in various aspects of facility and equipment validation and the implementation of a GMP QMS.
Adnan has supported us in mapping out our regulatory requirements and setting up our QMS. As a start-up company, we needed someone who could be flexible and provide expert knowledge of the industry. Adnan took the time to understand the needs of our company and would often go beyond expectations, forwarding us relevant links and research to aid our efforts. His support and guidance has been invaluable to us. It has been a pleasure working with Adnan and I would happily do so in the future and recommend his services to others.
Lantor has used Adnan’s services for the generation of protocol and report documentation in projects relating to primary package validation and stability testing of medical devices. He has an excellent knowledge of the necessary regulatory requirements and always makes a point of being available for meetings and discussions via teleconference. He has proven to be very professional, reliable and resourceful.