PCS is an expert on Quality Management Systems in the pharmaceutical industry. Through our unique approach of combining Quality Culture and Quality Systems we do not only ensure GMP compliance but a reduction in deviations, errors and ultimately costs!
Just compliance is a thing of the past. By connecting people to operational quality you will improve not only compliance but also decrease batch problems.
Accountability is key to assure quality. We support process ownership to inspire a more innovative and responsible working culture throughout all layers of the organization.
Focusing solely on documents alientates you from your core process. PCS helps you retake control of your value adding activities.
PCS supports the reporting of quality issues. Our consultants have the tools and experience to help you inspire quality defect reporting, benefiting both the company and employees.
Our Pharmaceutical Quality Management Systems have matured in terms of documentation and there is an ongoing struggle to reduce batch problems and deviations without increasing the amount of rules/procedures, supervision and QA personnel.
PCS is at the forefront of remedying this dilemma by employing Quality Culture initiatives which connect people to quality, centralize the core process(es) and stimulate a productive and innovative working environment.
PCS can support your organization with a myriad of services; from writing Standard Operation Procedures (SOPs), helping with Management Review Preparation, reviewing Batch Documentation, providing Quality Assurance Officers and Qualified Persons to restructuring and improving your entire Quality Management System.All our consultants are supported by a team of international experienced, and seasoned, experts. Knowledge is shared internally and resources are pooled to ensure you receive the most cost-effective solution. Is the service you require not listed on this page? Simply use the contact form at the top of this page to get in touch!
PCS can provide seasoned experts to tackle any GMP/GDP/GLP-related issue you may be encountering. With more than thirty years of experience in the pharmaceutical industry we have dealt with a myriad of situations, problems and challenges. You can view our recent experience here. Our experts will take on the existing workload and can catch up to any lapsed work if required.
Our consultants are experts in the fields of Good Manufacturing Practices, Good Distribution Practices, Good Laboratory Practices and current Good control Laboratory Practices for producers of Finished Products, Intermediates, Excipients and Active Pharmaceutical Ingredients. In addition PCS can assist the Food and Chemical industries with Quality Assurance related issues.
The list below represents the most common functions the consultants of PCS are requested to fulfill.
We believe that our principles are at the core of everything we do. As a client of PCS you may be assured that we will conduct every assignment with integrity.
We perform as promised and remain committed to delivering excellent customer service. You may depend on PCS to deliver quality; we will always provide an expert suited for the assignment.
As PCS promotes an efficient and honest working culture you may depend on us to have your best interests at heart, the essence of the problem will always be discussed.
During the execution of every assignment our experts will try to connect people and quality, creating an ideal combination for ensuring compliance with the leading regulations.
Our interim managers have performed a great number of assignments globally, in a range of industries.
We are a dedicated team of GxP experts who know all ins and outs of Quality Systems and its potential issues.
Our GxP experts work in a great number of companies across the pharmaceutical industry as Subject Matter Experts.
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