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Oxford provides services across the globe with dedicated offices in the countries listed below. If you need more information on specific services in your country, please contact us.

United States

Canada

Ireland

United Kingdom

Netherlands

Belgium

Germany

Switzerland

Experienced Consultants to Help
Meet Market Demands

With constant regulatory changes, technology advancements, and the need to drive innovative products to market, having the right partner for your project is essential. That’s why we connect you to the highest quality of talent for your staffing and consulting needs.

For a full overview of the industries that we serve, click here.

From discovery and formulation to process improvement, we have the experienced professionals you need to support your research and development tasks.

  • Product Development
  • Method Validation
  • Method Qualification
  • Analytical Development
  • Process Development
  • Formulation
  • Design Specification & Analysis
  • Quality Engineering

Learn more about our experience and how you can tap into our network for your specific initiative. Or, read industry insights and leverage additional resources on our blog.

Our consultants can support you on all laboratory related projects from planning, design, upgrade or management of laboratories to leading scientific and technological research, and conducting the experiments and measurements needed to ensure ‘product quality’.

  • Quality Control
  • Sample Preparation
  • Stability
  • LIMS
  • Microbiology
  • Life Sciences
  • Biotechnology/Molecular Biology
  • Analytical Chemistry
  • Leadership and Management
  • Sales
  • Product Specialists
  • Field Service Engineering
  • Lab Equipment Qualification

Learn more about our experience and how you can tap into our network for your specific initiative. Or, read industry insights and leverage additional resources on our blog.

When time is of the essence to get your product to market, our clinical research consultants can guide you every step of the way. We support clinical trials with a wide range of specialties.

  • Preclinical Studies
  • Early Phase Studies
  • Study Start Up/Feasibility Activities
  • Clinical Monitoring & Oversight
  • Clinical Quality and Regulatory Affairs
  • Contract & Budget Management
  • Clinical Study Nurses
  • Data Entry/Managers & Study Coordinators (site based)
  • Clinical Physicians

Learn more about our experience and how you can tap into our network for your specific initiative. Or, read industry insights and leverage additional resources on our blog.

Our medical consultants come from all types of medical backgrounds, meaning we can provide experts for all therapeutics areas.

  • Medical Affairs
  • Medical Information
  • Medical Writing
  • Market Access
  • Health Economics
  • Real World Data Management
  • Medical Advisor
  • Medical Manager
  • Medical Liaison

Learn more about our experience and how you can tap into our network for your specific initiative. Or, read industry insights and leverage additional resources on our blog.

Our consultants play a key role in the healthcare system through auditing, monitoring and discovery of interactions amongst drugs and their effects in humans.

  • EU- Qualified Person Responsible For Pharmacovigilance (QPPV)  / Local-QPPV
  • Periodic Safety Update Reports (PSURs) 
  • Development Safety Update Report (DSURs)
  • Risk Management Plan
  • Pharmacoepidemiology
  • Literature Searches

Learn more about our experience and how you can tap into our network for your specific initiative. Or, read industry insights and leverage additional resources on our blog.

In a regulated environment, having a flawless strategy and execution is imperative. Our consultants assist with planning, submissions, technical documentation, remediation and resolution management to help you meet regulatory requirements and deadlines.

  • Premarket Approvals (PMAs)
  • 510(k) Submissions
  • Investigational Device Exemptions (IDEs)
  • Investigational New Drug (IND) Applications
  • Biological License Applications (BLAs)
  • New Drug Applications (NDAs)
  • Chemistry, Manufacturing & Controls (CMC) Submissions
  • CE Mark
  • Adverse Event Reports (AERs)
  • European Medical Device Regulations (MDR)
  • In Vitro Diagnostic Medical Device Regulations (IVDR)
  • Clinical Evaluation Reports (CERs)
  • Inspection Readiness
  • ISO13485, ISO14971, IEC60601, IEC62304, 
  • ISO9001
  • 21 CFR Parts 4, 11, 210, 610 and 820

Learn more about our experience and how you can tap into our network for your specific initiative. Or, read industry insights and leverage additional resources on our blog.

Need support with your Engineering projects? Our consultants can help with CAPEX, Greenfield & Brownfield projects, expansions and technical transfers.

  • Commissioning, Qualification and Validation (CQV)
  • CAPEX Project Management
  • FMEA
  • Packaging and Labelling
  • Failure Mode and Effects Analysis (FMEA)
  • HVAC & Utilities
  • Process Engineering
  • Upstream and Downstream Process
  • Mechanical Engineering 
  • Electrical Engineering

Learn more about our experience and how you can tap into our network for your specific initiative. Or, read industry insights and leverage additional resources on our blog.

Looking for help with your supply chain and manufacturing operations? Our consultants can guide you through everything from sourcing and commodity management to logistics optimisation.

  • Product Assembly
  • Packaging & Labelling
  • Technology & Process Transfer
  • Lean 6 Sigma 
  • Process Development & Optimisation
  • Sterilisation & Purification
  • Automation
  • Supply Chain

Learn more about our experience and how you can tap into our network for your specific initiative. Or, read industry insights and leverage additional resources on our blog.

Our consultants can help validate products, equipment, systems, software, facilities, utilities, test methods, processes, and more.

  • Standard Operating Procedures (SOPs)
  • Master Validation Plans (MVPs)
  • Equipment Qualification
  • Cleaning Validation 
  • Analytical Test Method Validation
  • Verification & Validation 
  • Computer Systems Validation

Learn more about our experience and how you can tap into our network for your specific initiative. Or, read industry insights and leverage additional resources on our blog.

The right plans and processes are imperative to meeting your project requirements. Through our network of QA experts, we support clients in their quest to achieve unparalleled attention to quality with their highly regulated products.

  • Gap Assessment
  • Risk Mitigation & Management
  • Quality Systems Development/Improvement
  • Corrective & Preventive Action (CAPA)
  • Deviations Handling
  • Customer Complaints 
  • Training
  • Documentation
  • Auditing
  • Batch Review

Learn more about our experience and how you can tap into our network for your specific initiative. Or, read industry insights and leverage additional resources on our blog.

Do your systems meet requirements, such as 21 CFR Part 11 and EU Annex 11? We have the right talent specialised in supporting your technology based quality and compliance needs.

  • Program Management
  • Validation
  • Migration
  • Risk Mitigation
  • Implementation
  • Upgrades
  • Customization
  • Configuration
  • Quality Technology Agreements
  • Quality Management (QMS)
  • eQMS
  • Electronic Document Management (EDMS)
  • Laboratory Information Management (LIMS)
  • Electronic Laboratory Notebooks (ELN)
  • Scientific Data Management (SDMS)
  • Clinical Trial Management (CTMS)
  • Clinical Data Management (CDMS)
  • Learning Management (LMS)
  • Manufacturing Executions (MES)
  • Building Management (BMS)
  • Electronic Common Technical Docs (eCTD)
  • Data Integrity (DI)

Learn more about our experience and how you can tap into our network for your specific initiative. Or, read industry insights and leverage additional resources on our blog.

The clinical research data your organization creates is a very valuable resource. Whether it’s transforming, storing, or analysing and validating this data, every step is important. Our consultants can support you through the different steps and aspects of data management within a clinical trial.

  • Clinical Study Data Management
  • eCRF Design & Validation
  • Clinical EDC Application Development
  • Statistics
  • Biometrics

Learn more about our experience and how you can tap into our network for your specific initiative. Or, read industry insights and leverage additional resources on our blog.

Oxford can support you with all steps within the systems lifecycle from programming to commissioning and validation to compliance. We can also lead your IT roll outs to other sites and countries.

  • DCS
  • PLC 
  • MES
  • Allen Bradley/Siemens S7/Rockwell/Delta V
  • Software Development and Configuration
  • Manufacturing Automation
  • Machine Design
  • Development and Validation Process
  • Computer Systems Validation

Learn more about our experience and how you can tap into our network for your specific initiative. Or, read industry insights and leverage additional resources on our blog.

Testimonials

We're with You Every Step of the Way

People – Technology – Solutions

The Talent We Bring to the Table, that’s the Oxford Difference

Knowing that every project requires the right mix of expertise, we build each team to meet the needs of each project. We bring our breadth of services and depth of skills together to serve your industry, and to meet your biggest project challenges. With more than 35 years of experience, you can trust that when you work with Oxford you work with a group of people who bring expertise and understanding to the conversation, remain committed, and care about your success.

165 +
Life Sciences Organizations Supported
5000 +
Life Sciences Consultant Engagement Since 2000
1075 +
Consultants in Medical Writing & Regulatory Affairs
820 +
Employees Worldwide

Side-by-Side Builds Trust
and Delivers Results

Check out some of the latest projects that we’ve delivered for our clients.

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