Transforming Medical Discoveries

Navigating the evolving landscape of global regulatory requirements demands deep expertise, strategic foresight, and reliable talent. At TFS Staffing Group, we provide specialized staffing solutions and consulting support for companies seeking to meet FDA (U.S. Food and Drug Administration) and EMA (European Medicines Agency) compliance at every phase of the product lifecycle.

Whether you're preparing for pre-IND meetings, managing marketing authorization submissions, or responding to regulatory queries, we connect you with seasoned regulatory affairs professionals who understand both regional and international guidelines.

• Regulatory Strategy Development (US & EU)
   
• IND / CTA Preparation and Submission
   
• NDA / BLA / MAA / Variations / Supplements
   
• eCTD Publishing and Document Management
   
• Health Authority Interactions & Meeting Preparation
   
• Labeling Strategy and Review
   
• Post-Marketing Compliance and Lifecycle Management
   

• Regulatory Affairs Specialists and Managers
   
• Regulatory Affairs Consultants (US / EU / Global)
   
• Regulatory Operations and Submissions Professionals
   
• Labeling and CMC Regulatory Experts
   
• Global Regulatory Leads and Liaisons
   
• Quality and Compliance Advisors
   

Our candidates are well-versed in FDA, EMA, and ICH guidelines, bringing experience from small biotech to large pharmaceutical environments. Whether you require short-term project support or long-term strategic leadership, TFS Staffing Group ensures you’re equipped with professionals who understand the stakes and deliver results.

Regulatory excellence starts with the right people. Let’s get you there.

Expanding into international markets requires a nuanced understanding of regional regulatory frameworks. At TFS Staffing Group, we offer tailored staffing and consulting services for companies seeking regulatory approval and post-market compliance across Asia-Pacific (APAC) regions and other global health authorities.

From Japan’s PMDA and China’s NMPA to Australia’s TGA and Canada’s Health Canada, we supply regulatory professionals who are experienced in navigating the unique requirements, timelines, and communication standards of each agency.

• Japan (PMDA)
   
• China (NMPA)
   
• South Korea (MFDS)
   
• Australia (TGA)
   
• India (CDSCO)
   
• Brazil (ANVISA)
   
• Canada (Health Canada)
   
• Middle East & Africa (SFDA, SAHPRA, etc.)
   

• Global Regulatory Strategy and Market Access Planning
   
• Country-Specific Dossier Preparation and Submissions
   
• Clinical Trial Applications (CTAs) and Ethics Submissions
   
• Product Registration and Licensing Support
   
• Local Labeling Compliance and Translation Coordination
   
• Global Lifecycle Management
   
• Liaison Support with Local Regulatory Authorities
   

• Global Regulatory Affairs Associates and Managers
   
• APAC Regional Regulatory Leads
   
• Local Submission Specialists
   
• Multilingual Regulatory Consultants
   
• Quality and Pharmacovigilance Advisors
   

TFS Staffing Group bridges the gap between your innovation and global approval. Our professionals offer localized insight and global alignment to help accelerate access, reduce risk, and ensure sustained compliance worldwide.

Expand confidently — with strategic talent tailored to global succes

At TFS Staffing Group, we offer end-to-end Food Safety & Quality Consulting solutions tailored to the unique needs of organizations across the food production, life sciences, biotech, and nutraceutical sectors. We understand that food safety is not only a compliance requirement—it's a business-critical function that protects consumers, builds brand trust, and drives operational efficiency.

Our consultants are seasoned experts in regulatory compliance, quality systems, and risk management. We partner with manufacturers, processors, distributors, and service providers to ensure that your food safety and quality operations are built on a solid, proactive foundation.

✅ Regulatory Compliance Support
Expert guidance to help you meet and exceed FDA, USDA, FSMA, HACCP, and GFSI standards.

✅ GMP & GFSI Program Development
Design, implementation, and auditing of Good Manufacturing Practices and Global Food Safety Initiative-aligned systems.

✅ Third-Party & Internal Audit Preparation
We help you prepare for and navigate audits and inspections—both internal and external.

✅ Supplier Verification & Risk Mitigation
Evaluation of suppliers, raw materials, and transport logistics for potential safety risks.

✅ Food Labeling & Allergen Control
Compliance consulting for product labeling, allergen declarations, and nutritional accuracy.

✅ Sanitation Program Development
Custom sanitation SOPs, SSOPs, and environmental monitoring programs for continuous facility hygiene.

✅ Recall Planning & Crisis Management
Development of recall protocols, mock recall exercises, and crisis communication strategies.

✅ Workforce Training & Certification
On-site and virtual food safety training programs for line workers, supervisors, and managers.

• Food & Beverage Manufacturers
   
• Nutraceutical & Dietary Supplement Companies
   
• Agricultural & Animal-Based Product Producers
   
• Ready-to-Eat and Perishable Food Processors
   
• Cold Storage & Distribution Facilities
   

• Food Safety Consultants
   
• FSQA Directors
   
• HACCP Coordinators
   
• Sanitation & Hygiene Managers
   
• GFSI Implementation Experts
   
• Quality System Auditors
   
• Labeling and Regulatory Specialists
   

Whether you're launching a new product line, preparing for certification, or building a quality-first culture from the ground up, TFS Staffing Group delivers the expertise to elevate your operations and exceed regulatory expectations.

Food safety isn’t optional. It’s foundational. Let’s build it right—together.
 

We provide highly skilled professionals across all phases of clinical trials, regulatory affairs, quality assurance, medical affairs, pharmacovigilance, and more. With over 20 years of experience in life sciences staffing, we understand the unique challenges of sourcing niche talent in a competitive market. Our recruitment specialists are trained to identify, vet, and place professionals who are not only qualified but also aligned with your company’s mission and values.

Our Talent Acquisition Solutions Include:

• Permanent Placement
   
• Contract & Freelance Staffing
   
• Executive Search
   
• Functional Outsourcing (FSP)
   

We go beyond resumes. We deliver people who can make a difference from day one.

Expert Insights to Navigate Complex Challenges

Our Life Science Consulting division offers strategic support and specialized expertise across regulatory compliance, clinical operations, quality systems, data management, and commercialization strategies. Whether you’re launching a Phase I trial or preparing for regulatory submission, we connect you with consultants who bring real-world industry knowledge and measurable results.

Our Consulting Services Cover:

• Clinical Trial Management
   
• Regulatory Submissions & Strategy
   
• Quality & Compliance Optimization
   
• Medical Writing & Safety Reporting
   
• Market Access & Commercial Strategy
   

We tailor every engagement to your project scope, timeline, and budget — helping you accelerate success while mitigating risk.

At TFS Staffing Group, we understand the critical role that specialized talent plays in the success of clinical trials. From early-phase research to late-stage development, our Clinical Trial Staffing solutions are designed to support pharmaceutical, biotechnology, and medical device companies with the right professionals at every stage of the trial lifecycle.

Our team delivers high-quality, pre-vetted candidates with experience in global trials, regulatory compliance, GCP standards, and therapeutic-area expertise — enabling faster timelines, better data quality, and fewer delays.

• Clinical Research Associates (CRAs)
   
• Clinical Trial Managers (CTMs)
   
• Clinical Project Managers
   
• Clinical Operations Directors
   
• Medical Monitors & Safety Physicians
   
• Regulatory Affairs Associates
   
• Biostatisticians & Statistical Programmers
   
• Data Managers & Clinical Data Analysts
   
• Trial Assistants, Study Coordinators & Site Support
   

• Oncology
   
• Cardiovascular
   
• Central Nervous System (CNS)
   
• Dermatology
   
• Infectious Disease
   
• Rare Diseases
   
• Ophthalmology
   
• Immunology
   
• And more
   

Whether you require permanent hires, contract staff, or full-function outsourced teams, we tailor our services to meet your timeline, budget, and regulatory needs.

From Phase I to Phase IV — we bring the people who power progress.

Navigating the complex and evolving landscape of global regulatory requirements demands precision, expertise, and agility. At TFS Staffing Group, we provide end-to-end Regulatory Affairs Support to help life science companies bring their products to market efficiently and in full compliance with regional and international standards.

We connect you with experienced regulatory professionals who understand submission strategies, compliance frameworks, and the dynamic regulatory expectations of health authorities such as the FDA, EMA, MHRA, Health Canada, and others.

• Regulatory Affairs Staffing: Associates, Managers, and Directors
   
• FDA & EMA Liaison Support
   
• IND, NDA, BLA, MAA Preparation & Submission
   
• Regulatory Strategy Development for Drug & Device Approvals
   
• Chemistry, Manufacturing & Controls (CMC) Documentation
   
• Labeling & Promotional Material Compliance
   
• Post-Market Surveillance and Global Variations
   
• Risk Management & GxP Compliance Consulting
   
• Orphan Drug Designation & Accelerated Pathways Guidance
   

Whether you're a startup preparing for your first filing or a global enterprise managing a complex product portfolio, our regulatory experts help ensure your products meet approval standards and stay compliant throughout their lifecycle.

Partner with TFS Staffing Group for regulatory clarity, operational confidence, and faster approvals.

At TFS Staffing Group, we understand that clear, accurate, and compliant communication is vital at every stage of the drug and device development process. Our Medical Writing and Communications services connect you with seasoned professionals who specialize in transforming complex scientific data into precise, regulatory-compliant, and audience-tailored content.

Whether it's regulatory documentation, clinical study reports, or scientific publications, our writers ensure that your data is presented with clarity, scientific integrity, and strategic intent.

• Medical Writers (Regulatory & Clinical)
   
• Scientific Directors & Medical Communication Managers
   
• Publication Managers & Medical Affairs Specialists
   
• Health Economics and Outcomes Research (HEOR) Writers
   
• Market Access Writers
   
• Editorial & Quality Review Specialists
   
• Medical Science Liaisons (MSLs)
   

• Clinical Study Protocols, Investigator Brochures (IBs), and CSRs
   
• Regulatory Submission Documents (INDs, NDAs, MAAs, etc.)
   
• Scientific Abstracts, Posters, and Manuscripts
   
• Patient-Facing Education Materials
   
• Medical Information Letters and Standard Response Documents
   
• Slide Decks, Product Monographs, and Training Content
   
• Evidence-Based Value Dossiers and Payer Communications
   

Our communication experts are well-versed in ICH, GPP, and AMA guidelines, and work closely with clinical, regulatory, and commercial teams to ensure consistency and quality across all deliverables.

From bench to bedside — we articulate science with clarity and purpose.