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.
Learn about our COVID-19 partnership with Life Sciences organizations.
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
- mRNA
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
- Biotechnology/Molecular Biology
- Analytical Chemistry
- Leadership and Management
- Sales
- 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.
- CER Writing
- Bioinformatics
- 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
- 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.
We have solutions to help you meet daily demands while enhancing growth and innovation for your organization.
- ERP (SAP™, Oracle™, Microsoft Dynamics 365™/Microsoft Dynamics™, PeopleSoft™ & JDE™)
- Organisational Change Management (OCM) and Training
- Infrastructure & Security
- Cloud Technology (AWS™/Azure™)
- Big Data & Analytics
- Digital Transformation
- CRM & SFDC/Salesforce
- Master Data Management
- HR Cloud Solutions
- Manufacturing Execution System (MES)
- Warehouse Management Solutions Including Advance Track & Trace for Pharmaceuticals/ATTP
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.
Scope and Objectives
Oxford Global Resources started a partnership with a multinational pharmaceutical company in 2018. Over the years, due to the quality outcomes, our teams have delivered, the client decided to make us an exclusive partner dedicated to supporting and guiding all medical education services across the organization, including the provision of a comprehensive service, responsibility for planning, delivery, and evaluation of professional programs in terms of operational outcomes, continuing professional development, induction, and skills training for juniors and trainees
Scope and Objectives
Oxford Global Resources started a partnership with a multinational pharmaceutical company in 2018. Over the years, due to the quality outcomes, our teams have delivered, the client decided to make us an exclusive partner dedicated to supporting and guiding all medical education services across the organization, including the provision of a comprehensive service, responsibility for planning, delivery, and evaluation of professional programs in terms of operational outcomes, continuing professional development, induction, and skills training for juniors and trainees.
Discover how Oxford provided the right talent to support a client’s global clinical trials.
A leading international pharmaceutical company was launching a vaccine for the COVID-19 virus and needed technical transfer and GxP support.
We assisted with Commissioning, Qualification, and Validation (CQV) support for a new facility expansion to support our client’s rapid growth. Learn how we delivered in spite of challenges.
A vocational university created a committee to assist their lab education department. Learn how Oxford provided invaluable perspective.
When our client needed to develop, manufacture, and distribute the COVID vaccine quickly and with high-quality results; they reached out to Oxford Global Resources for support.
AZ Sint-Maarten conducted a clinical trial for a COVID-19 vaccine. Due to the volume of volunteers, they would need more staff for an effective trial.
The COVID-19 pandemic required all governments, organizations, and individuals to work together in unprecedented ways. Discover how Oxford's support allowed an international testing laboratory to contribute to the Netherlands' efforts against the pandemic.
In the global efforts against COVID-19, widespread testing is key. Learn how Oxford helped Biogazelle quickly find the right talent to accommodate a large-scale testing initiative.
Our client, needed to convert more than 3,000 2D and 3D drawings and related specs of archived orthodontic products from a legacy Pro E CAD tool to SolidWorks™. With Oxford's partnership, learn how they achieved their goals.
In the fight against COVID-19, many organizations were asked to go above and beyond to help. One diagnostic organization was tasked by the government to assist in testing samples. Learn how Oxford helped them achieve their maximum daily capacity.
Discover how Oxford’s eight-year partnership with a CMO Management group allowed them to consistently achieve goals and expand their business.
Discover how Oxford assisted a microbiological testing company complete a backlog of analyses and uphold its commitments to its clients.
In order to pass an upcoming FDA inspection, our client needed specialized support. Discover how Oxford's partnership made the difference.
Discover how Oxford’s team of medical writers completed 150 scientific validity reports within five months.
Discover how Oxford helped a pharmaceutical manufacturer open a fully validated facility within eleven months.
A medical device manufacturer was in need of installing and qualifying a completely new piece of automated manufacturing equipment. Learn how Oxford's experts helped our client create a compliant system.
Discover how Oxford’s talent helped meet the deadline and complete the facility expansion.
Discover how Oxford promptly provided 15 consultants that were critical to achieving an observation-free site inspection.
Discover how Oxford’s consultants helped to remediate the issue and pass the FDA re-inspection.
Discover how Oxford provided assistance to keep the project on track.
Discover how Oxford consultants revised a Quality Management System to meet FDA regulations within seven weeks.
Discover how Oxford’s team helped create an FDA-compliant automated production process.
Discover how Oxford’s team quickly helped capture and address issues to achieve full compliance.
Discover how Oxford’s team of experts completed product-specific and State-of-the-Art Literature Searches within four months.
Discover how the right Oxford consultants were able to provide support for a Data Integrity Remediation project when a client needed niche expertise.
Discover how Oxford’s expert consultants enabled a smooth production process by reviewing six months of inaccurate data.
Discover how Oxford helped our client qualify 50 combination products in 3 years.
Discover how Oxford helped a medical device manufacturer start their MDR compliance journey the right way.
Due to a facility expansion, a global pharmaceutical manufacturer needed to engage with an organization that could provide Commissioning, Qualification and Validation services. Learn how Oxford delivered.