- Training and guidance for GMP compliance and certification of the facility
Continued compliance with Good Manufacturing Practices is an ever
challenging task in all segments of pharmaceutical business.
Development of in-house skills is a laborious and expensive process.
Our partners experts will provide to our customers the services of GMP training
and guidance in a time and cost-effective manner.
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Preparation, adapting and training related to the documentation in all areas of pharmaceutical manufacturing
Continuously changing regulations and the increasingly demanding
complexity of the pharmaceutical manufacturing require highly
experienced specialists. Our customers may take advantage of the expertise of our partner`s pharmaceutical experts in preparing the corresponding documentation for
all areas pharmaceutical manufacturing.
- Layout design of the facility, sterile areas and laboratories and their internal organization
The design and layout of the factory, sterile areas and laboratories
in accordance with GMP and GLP regulations are the basis of a
profitable pharmaceutical company. Through our highly experienced and
trained collaborators, QPS is ready to assist any concerned company in
setting up a modern, GMP certified facility, starting with its design
and internal layout, machinery and equipment.
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GMP auditing of any manufacturing for API’s, finished pharmaceutical formulations and contract manufacturing facility.
In today's world of strict regulations from authorities and
challenging business and regulatory demands regarding GMP
certification, more and more companies are outsourcing theses services
of GMP auditing, which offer them significant time & cost advantage
while keeping their staff focused on other important projects.
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Consulting and advisory services related to equipment and machinery
Benefiting of our close collaborators’ experience in production of
almost all pharmaceutical formulations, QPS is able to recommend to
concerned customer the best machines and equipment, tailored on
client’s needs and particular projects.
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Start-up guidance and consulting
Starting up of a manufacturing facility with validations is a
challenging area and we are offering our experts’ services to
manufacturing units, both for APIs and for finished dosage forms.
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