- Mon - Sat: 9.00 AM - 6.00 PM
- tatasantosh@gmp-pharmatech.com
- +91 87900 46880
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AHU & Clean Room zoning critical to prevent Contamination are critical Utilities
about GMP Pharma consultants
GMP Pharma 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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Improve Your Business We Offer the following
We Offer the following
Pharmatech Services
Project Planning
Designing a pharmaceutical manufacturing layout involves a systematic approach to ensure that the facility meets regulatory requirements, supports efficient production processes, and maintains product quality.
AHU Zoning and Validations
Clean rooms must ensure proper airflow, pressure differentials, contamination control, and ease of maintenance. Designing the layout for an AHU (Air Handling Unit)
Equipment & Qualifications
Designing pharmaceutical equipment and utilities is a critical aspect of creating a manufacturing facility that meets stringent regulatory requirements, ensures product quality, and supports efficient operations.
Audits & Compliance
AUDITS & COMPLIANCE Pharmaceutical vendor audits and compliance are critical components of the quality management system in the pharmaceutical industry. These audits ensure that suppliers and service providers
Computer System Validations
Computer System Validation (CSV) is a process used to ensure that computerized systems used in pharmaceutical manufacturing and quality processes are functioning according to their intended purpose and meet regulatory
Training
Computer System Validation (CSV) is a process used to ensure that computerized systems used in pharmaceutical manufacturing and quality processes are functioning according to their intended purpose and meet regulatory
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Training and Development
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Our Reviews
"Hi, my self Subhani Shaik working as manager-QA. We engaged GMP team in 2016 for upgrading our compliance on primary packing systems and induction seals. Their guidance helped us achieve customer satisfaction and regulatory compliance. Association with them is a great learning experience that we cherish even today."
Subhani Shaik
"I have come across this team, when we have hired a consultancy for GMP training from expert from the industry to train the trainers as well as the doer. The team is very much professional and knowledgeable having excellent problem solving skills and knowledge of current Good Manufacturing Practices of Sterile, non sterile formulation as well as API’S."
Gopichand Chaphekanade
"Hi I am Arun having 20 years of experience in API quality assurance, when I was working with my previous organization I am very much closely associated with this GMP consultancy team, they supported in improvising the quality systems. The team has vast knowledge in all sectors pharmaceutical systems."
Arun Karanam
"Excellent team and having Technically strong resources. Providing best services to up keep the facility in GMP/regulatory compliance mode."
Raveendra A
I am happy to share my company’s exceptional experience working with Mr. S Parthasarthy and his team. Their expertise as a pharma quality consultant has been transformative for our organization.
Mr. S Parthasarthy has played a pivotal role in enhancing our quality systems by aligning them with ICH guidelines. Their meticulous approach to improving our processes has not only elevated our quality standards but has also ensured that our systems are robust and compliant.
The training sessions provided by to our quality and production staff were invaluable. Their ability to convey complex concepts in an understandable manner has significantly boosted our team's competency and confidence. This has directly contributed to our success in passing customer audits with flying colours.
Overall, M/s GMP Pharmatech Consultants has been instrumental in advancing our quality practices, and their contributions have set a new benchmark for excellence within our organization. We highly recommend M/s GMP Pharmatech Consultants to any company seeking to enhance their quality systems and achieve regulatory compliance with a high level of professionalism and expertise.