GxP Central places a premium on the importance of continuous compliance monitoring to ensure that your efforts are both current and effective. Our consultants possess extensive domestic (US) and global experience and can cover the entire supply chain from raw materials to finished products.
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GxP Central's Quality Management Consultancy and Auditing Services which are based on highly specific quality management plans. Our team of highly experienced consultants which can help you with the evaluation, review, setting-up and implementation of QM systems in client companies.
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In-depth and specific quality procedures help an organization remain compliant while avoiding the unnecessary expense of product redesign and reformulation. Clear quality procedures also ensure that every person involved in the product is appropriately trained and knowledgeable about roles, responsibilities and regulations.
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Our services deliver distinct advantages to the manufacturers of finished pharmaceuticals and components. We have in-depth knowledge of 21 CFR Part 11, as well as the regulated process equipment and the GMPs of regulatory agencies.
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‘Strong emphasis on Confidentiality and Transparency
GXP Central’s services are girded by an emphasis on quality standards, attention to detail and longstanding relationships with our clients. We are dedicated to conducting our work in a transparent manner to ensure that activities are always ethical, and that there is never a conflict of interest.
Equally, GXP Central understands the importance of confidentiality and treat the information our clients share with complete discretion. GXP Central’s confidentiality agreements are in place to protect clients as well as other stakeholders including the general public. The highest ethical and confidentiality standards are maintained at all times.
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has over 20-plus years of pharmaceutical experience. Brock began his career as a staff clinical hospital pharmacist, working in a...
Quality Assurance Consultant Available for consultation: audits, remediation, QMS planning and change, in-house training and personnel systems management advisor. EU...
Elizabeth is a Clinical Research professional who is a Registered Nurse with a Post Graduate qualification in Pharmaceutical Science and...
has vast experience with over 12 years in the research industry successfully completing audits, FDA inspection preparation and assistance, monitoring...
provides expertise in a variety of areas. She is certified as a clinical research auditor and performs research department compliance...
Rahul has over 20 plus years of pharmaceutical experience He has led IND, NDA and ANDA projects from the stages...
Over the last decade we have contributed to the success of many Biotech and Pharmaceutical companies, helping them to meet the challenges of product development, registration and approval, and to maintain and grow their products during lifecycle management
With an array of expertise, our staff understands your unique challenges and concerns faced in a highly regulated environment. We take the time to understand your goals and limitations to provide you the best solutions. Assembling QA and Regulatory professionals with a vast knowledge base ensures that each project is handled with your unique concerns, challenges, goals, and limitations in mind.
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Quality Resource Solutions, LLC 5550 Painted Mirage Road, Suite 320-A089 Las Vegas, NV 89149
800 921 3157 info@gxpcentral.com