Contracting
GxP Consulting can provide you with the contract support you need in order to comply with the regulatory requirements of the MHRA, FDA, EMEA, WHO and ICH. Our contact team is highly skilled and experienced in identifying, communicating, managing and delivering your Good Manufacturing Practice (GMP), Good Automated Manufacturing Practice (GAMP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP) and Good Distribution Practice (GDP) requirements.
GxP Consulting has been providing contract services to the Pharmaceutical, Biotechnology (BioPharma), Consumer Healthcare, Medical Device, Homeopathic and Veterinary industries for many years. We offer the full suite of contracting services to either the contractor looking for project work or for the employee looking to hire fully managed contractors for short-term or long-term projects. Services include full-time, part-time and interim contract support options.
Our service – managed deliverables not contractor placement
Our customers use our contract services because we are focussed on what you need – to deliver a quality service against a defined budget and timescale. We provide you with a fully-managed service that minimises your time spent managing contract support. Benefits we offer you include the option to use specific members of our team to complete specific tasks based upon skill-sets and experience.
GxP Consulting has established an enviable reputation for delivery of contract services based upon trust, professionalism and value. This is supported by our long-term and repeat business with practically all customers the company has ever worked with.
Services Provided
GxP Consulting can provide your business with contract support for GxP jobs in the following areas:
- Validation Engineers
- Validation Scientists
- Computer Validation Specialists
- Technical Writers
- Quality Managers
- Quality Assurance (QA) Staff
- Quality Control (QC) Staff
- Clinical Trial Managers (CTM)
- Project Managers
- Regulatory Compliance Staff
- Document Managers
