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about GMP Pharma consultants

GMP Pharmatech consultants serves Small and Medium Enterprises

GMP Pharmatech consultants has been promoted by professionals with over 100 years of cumulative experience in the Pharmaceutical Industry.


Mr. S. R. Parthasarathy has over 55 years of experience. His initial experience was from M/s Pfizer (Erstwhile M/s Parke Davis) and has over 30 years of consulting experience. He has toured many countries such as China, Chile, Brazil, West Africa, Malaysia , The Philippines, Nepal, Denmark , Netherlands etc. He has understanding of national and international requirements.

Mr. Tata Santosh has over 23 years of experience. He is an expert on Quality Risk Management, Process Validations, Analytical Development, Process analytical technologies etc. He has conducted over 150 audits spanning Intermediates, Bulk APIs, Sterile and non-sterile formulations, Primary and secondary packaging systems.

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about GMP Pharma consultants

GMP Pharma consultants

GMP Pharma consultants have been promoted by seasoned Pharmaceutical professionals who have rich experience in all aspects of Pharmaceutical operations.
GMP Pharma consultants serves Small and Medium Enterprises, as well as large Pharmaceutical organizations who are involved in the manufacture of:
Intermediates & APIs
Formulations (both sterile and non-sterile)
Ayurveda
Excipients
Packing materials
Homeopathic products
Food product manufacturers
Public testing laboratories.
Medical Devices
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about GMP Pharma consultants

GMP Pharma consultants

They have the necessary wherewithal to provide all the services that are required to maintain a pharmaceutical industry in a perpetually compliant state by providing all the services that are required such as:
Quality System upgradation to meet national & international regulations
Training
Auditing
Validations
Preparation of dossiers
Answer all queries from regulatory authorities
reliable & safe

Our Strategy Development

"Our mission is to deliver exceptional pharmaceutical quality inspection and consulting services that ensure compliance, enhance product quality, and promote patient safety. We are committed to providing expert guidance, leveraging industry-leading practices, and fostering continuous improvement to help our clients navigate regulatory complexities and achieve operational excellence. Through our dedication to integrity, innovation, and client partnership, we strive to be a trusted advisor in the pursuit of excellence in the pharmaceutical industry."
"To be the leading global partner in pharmaceutical quality inspection, ensuring that our clients consistently meet and exceed the highest standards of safety, efficacy, and regulatory compliance. We aim to empower pharmaceutical companies through expert guidance, innovative solutions, and unwavering commitment to quality, contributing to the advancement of global health and patient safety."
"We at M/s GMP Pharmatech Consultants are unwaveringly committed to providing exceptional quality inspection consulting services to the pharmaceutical industry. Our dedication is rooted in ensuring that our clients meet and exceed regulatory standards while maintaining the highest levels of product safety, efficacy, and compliance.
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Solutions

Why Choose Us

Expertise and Integrity

Our team of seasoned professionals brings deep industry knowledge and a commitment to ethical practices, ensuring that every inspection is conducted with the utmost integrity and thoroughness.

Client-Centric Solutions

We tailor our consulting services to meet the unique needs of each client, offering customized solutions that drive operational excellence and foster long-term success.

Regulatory Excellence

We stay at the forefront of regulatory changes and industry trends, providing our clients with accurate and timely guidance to navigate complex compliance landscapes.

Continuous Improvement

We are dedicated to ongoing learning and innovation, continuously enhancing our methods and approaches to deliver the most effective and efficient inspection solutions.

Partnership and Support

We view every client relationship as a partnership, offering proactive support, clear communication, and a collaborative approach to achieving mutual goals.

Commitment

Through our commitment, we aim to contribute to the advancement of global health by ensuring that pharmaceutical products are of the highest quality and meet all necessary regulatory requirements."

what we do

Creating Your Startup Business

We help you see the world differently, discover opportunities you may never have imagined and achieve results that bridge what is with what can be.

our team

Our Proffesionals

Monica Black
chief communication officer
Peter Perish
chief business project
Olivia Woodson
international consultant
Peter Adams
co-founder of company
main principles

Frequently Asked Questions (FAQ)

What services do GMP Pharmatech Consultants offer?
We offer a comprehensive range of services, including GMP compliance audits, Quality Management System (QMS) development, process and equipment validation, regulatory support and submissions, GMP training, facility design and qualification, risk management, and supply chain management. Our goal is to ensure your operations are fully compliant with global GMP standards.
What industries do you serve?
We primarily serve the pharmaceutical, biotechnology, and medical device industries. Our expertise spans across manufacturing, quality assurance, regulatory affairs, and supply chain management, making us a valuable partner for companies of all sizes in these sectors.
How do you ensure confidentiality and data security?
We take confidentiality and data security very seriously. All client information is handled with the utmost care, and we implement strict data protection protocols to ensure that your sensitive information remains secure. We also sign non-disclosure agreements (NDAs) with our clients to formalize our commitment to confidentiality.
Can you help us prepare for regulatory inspections?
Absolutely. We specialize in inspection readiness and can assist you in preparing for inspections by regulatory bodies such as the FDA, EMA, and other international agencies. Our services include mock audits, documentation review, staff training, and ongoing support to ensure you are fully prepared for a successful inspection.
Do you offer customized solutions?
Yes, all of our services are tailored to meet the specific needs of each client. We understand that no two companies are the same, so we take the time to understand your unique challenges and goals before developing a customized plan that addresses your specific requirements.
How do you approach process validation?
Our approach to process validation is thorough and systematic. We start with a detailed risk assessment to identify critical process parameters. Then, we develop validation protocols (IQ, OQ, PQ) and oversee the execution of these protocols to ensure that your processes are robust, repeatable, and compliant with GMP standards.
What kind of training do you provide?
We offer a wide range of GMP training programs tailored to different levels within your organization. This includes introductory courses for new employees, specialized workshops for quality assurance teams, and regulatory updates for senior management. Training can be delivered on-site, online, or in a blended format to suit your needs.
How long does a typical consulting project take?
The duration of a consulting project varies depending on the scope and complexity of the work involved. After an initial consultation, we provide a detailed project plan with estimated timelines. We work efficiently to meet your deadlines while ensuring thoroughness and quality in our work.
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