Hire the Best Regulatory Compliance Freelancers
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I am a legal professional with extensive experience across corporate, transactional, and dispute-resolution work. My practice focuses on supporting businesses with contract drafting and review, commercial documentation, regulatory compliance, and corporate advisory, along with experience in civil and commercial litigation. I also provide high-quality legal research and legal writing services, including preparation of legal memoranda, issue briefs, contract analyses, and regulatory summaries, tailored to business and professional requirements. As a freelancer, I offer clear, practical, and business-oriented legal support to startups, SMEs, and international clients. My services are available for contract drafting and review, legal research and writing, compliance advisory, transactional support, and structured legal documentation. I work remotely, deliver concise and well-organised outputs, and focus on solutions that are legally sound and commercially effective. Clients can engage my services on a project basis or for ongoing legal support, depending on their needs.

PhD | Chief Formulation Chemist | Product Safety & Cosmetic Compliance Expert EU/UK/USA/MoCRA/CAN/AUS/UAE/ASEAN Are you planning to develop and sell your products legally in international markets such as EU, UK, USA, Australia, New Zealand, UAE, KSA, Korea, or on global online platforms and needs required documents like CPSR, PIF, SDS, Complaint Label, Certificates, MoCRA Dossier, AICIS categorization, CNF and UAE portal Registeration? Do you need products that are not only effective but also fully compliant with regulatory requirements of these regions? Or are you looking for customized formulations that are scientifically designed and ready for market approval? Or are you seeking for Regulatory Affairs Consultant for above global markets for handling compliance issues? You are in the right place. I am a PhD in Chemistry with more than 17 years of practical experience in cosmetic, nutraceutical, herbal, and skinceutical product development, safety assessments, toxicological risk assessments and regulatory Affairs. I have worked extensively on formulation design, safety assessment, toxicological evaluation, and regulatory compliance for global markets. My work is focused on helping brands, manufacturers, and online sellers create products that are safe, effective, and accepted by regulatory authorities and marketplaces. I work as a professional COSMETIC SAFETY ASSESSOR (Degrees recognition official certificates issued by USA, EU & UK ENIC NERIC) and FORMULATION CHEMIST. I have my own laboratory facility where I develop and test formulations through trial batches, optimization, and performance evaluation. My approach is based on scientific understanding of ingredients, their biological activity, and their safety profile, so the final product is not only compliant but also performs well in the market. I also have a team of qualified professionals including a pharmacist, medical doctor, and chemists who support in product development and evaluation. If required, I can also work through a UK registered safety assessment company, and verification details can be provided. My Services Include: 1. REGULATORY & SAFETY ASSESSMENT SERVICES CPSR & PIF (Cosmetic Product Safety Report & Product Information File) SDS preparation (CLP / REACH / ICH compliant) Toxicological risk assessments CPNP & SCPN notifications MoCRA (USA FDA) compliance support AICIS (Australia), EU, UK, Canada, ASEAN, UAE, KSA compliance GPSR risk assessments for general products Responsible Person (EU/UK/USA) services All safety assessments are conducted with scientifically, regulatory alignment, and full documentation readiness, ensuring smooth approvals and market acceptance. 2. SCIENCE-BACKED FORMULATIONS Cosmetics & Skincare (Complete range) Haircare (anti-hair fall, growth serums, scalp treatments, conditioning systems) Nutraceuticals & herbal products Cosmeceuticals / skinceuticals My formulations are developed based on: Bioactive metabolites (polyphenols, peptides, flavonoids, plant actives) Mechanism-based pharmacological action Scientifically validated ingredient synergy Each formulation is science-backed, effective, and market-ready, not just cosmetic blending. 3. SCIENTIFIC & EFFICACY BASED DEVELOPMENT Formulation design based on biological activity and active delivery systems Use of polyphenols, peptides, and advanced actives for targeted performance In vitro and in vivo testing support for product efficacy Performance validation based on real biological outcomes Laboratory & Testing – All Under One Roof TESTING FACILITIES I provide a complete in-house facility including: Trial batch development & pilot-scale runs Product optimization and scale-up readiness Stability and compatibility testing Microbial quality testing Preservative efficacy (challenge testing) Physical and chemical analysis Heavy metals testing Packaging compatibility test Marketplace Compliance Support FULL SUPPORT ON PRODUCT APPROVALS: Amazon Etsy Shopify eBay Other global e-commerce platforms WHY CHOOSE ME? All-in-one solution: safety assessment + formulation + testing + compliance Expertise in bioactive-based formulations (polyphenols & peptides) Own laboratory for real product development and validation In vitro efficacy support Strong integration of science and regulatory compliance Experienced multidisciplinary team (Pharmacist, Medical Doctor, Chemists) Unlimited regulatory support after project completion I have extensive experience working in ISO 9001, ISO 14001, ISO 17025, ISO 45001, and GMP-certified environments, ensuring international quality standards. My work focuses on delivering safe, effective, scientifically justified, and fully compliant products with strong regulatory acceptance. What You Get 1.Regulatory-ready documentation 2.Science-backed formulations 3.Proven efficacy approach 4.Smooth marketplace approvals 5.Complete product lifecycle support 6. All required documents and test reports All services under ONE ROOF

🏆🎖️ Top Rated Plus Upwork Freelancer 👋 Hi, I’m Saif Ur Rehman, Certified ISO & HSE Consultant and Qualified Engineer with a strong reputation for delivering high-impact compliance solutions, Audit-ready documentation, and tailored ISO Management systems across diverse companies. With a passion for excellence and a deep understanding of International Standards, I help businesses achieve operational efficiency, regulatory compliance, and sustainable growth through expertly crafted ISO, HSE, WHS, and risk management framework all documentation. 📌 My Services 📄 ISO Documentation, Gap Analysis, Implementation & Certification ✅ Manuals | Policies | QAQC docs | ITPs & ITCs | SOPs with templates | Flowcharts | Audit Checklists ✅ Internal/External Audits | Risk Registers | Gap Assessments ✅ Full IMS & ISMS compliance: QHSE + Information Security Management System 🛡️ HSE, ESG & Risk Management ✅ JSA | SWMS | RAMS | SDS | Incident Statistics ✅ Method Statements | HSE Plans | Technical Training | NDIS Compliance documentation ✅ WHS / OSHA / NEBOSH / GradIOSH-Compliant Support 📝 Technical & Research Writing ✅ Bidding Documents | Reports | Research Papers | Thesis 🎓 Certifications & Expertise ✅ ISO 9001:2015 (Quality Management System - QMS) ✅ ISO 27001:2022 (Information Security & Cyber Security - ISMS) ✅ ISO 14001:2015 (Environmental Management System - EMS) ✅ ISO 45001:2018 (Occupational Health & Safety - OHS) ✅ ISO 13485:2016 Medical Devices QMS ✅ ISO 22301:2019 (Business Continuity Management System - BCMS) ✅ ISO 17025:2017 (Laboratory Management System - LMS) ✅ ISO 22000:2018 (Food Safety Management System - FSMS & HACCP Plans) ✅ ISO 31000:2018 (Risk Management) ✅ ISO 50001:2018 (Energy Management System – EnMS) ✅ ISO 41001:2018 (Facility Management System - FMS) ✅ ISO 20000:2018 (IT Service Management System – ITSMS) ✅ ISO 42001: 2023 (Artificial Intelligence Management System – AIMS) ✅ ISO 20121:2024 (Event Sustainability Management System - ESMS ✅ ISO 26000, 26030:2019 & 14064 GHG ✅ NVQ Level 6 GradIOSH Occupational Health & Safety ✅ NEBOSH International General Certificate (IGC) ✅ Occupational Safety & Health (OSHA) ✅ cGMP & FDA 21 CFR Part 820 & 111 ✅ SOC 2 & HIPAA 🔷 Partnering with top certification bodies like ASIB, UKAF, UKAS, UAF, IAS, JAS-ANZ, and IAF. I help organisations achieve compliance, streamline operations, and meet global standards for long-term success. 🚀 Why Choose Me? ✨ Top Rated Plus – Trusted by global International clients ⏱️ Fast delivery – On-time & detail-focused 📈 Quality-driven – Customized & audit-ready documents 🌍 Industry-experienced – Engineering, Manufacturing, IT, Pharma 📩 Let’s Collaborate! I can perform quality projects. Feel free to contact me for more details. SAIF UR REHMAN

Medical Devices Expert / ISO 13485 / ISO 14971 / FDA / MDR / SaMD | EU MDR, FDA, SFDA, CE & Technical Files | PRRC I am a Senior Regulatory Affairs Consultant with 8+ years of hands-on experience in global medical device compliance. I specialize in guiding high-risk devices, Class III implantables, IVDs, SaMD, and combination products through EU, FDA, SFDA, UKCA, TGA, and DRAP regulatory pathways, ensuring audit-ready documentation, compliance, and timely market approvals. I provide end-to-end regulatory solutions, including device classification, technical documentation, regulatory submissions, post-market surveillance, risk management, and PRRC services. My goal is to help companies navigate complex regulations efficiently while maintaining the highest standards of safety and performance. 🌐 Global Regulatory Expertise: 🔹 EU MDR 2017/745 – CE marking, Technical Documentation, EUDAMED registration, UDI compliance, PRRC services (Article 15) 🔹 US FDA – 510(k) submissions, Quality System Regulations (21 CFR Part 820), post-market compliance 🔹 SFDA (Saudi Arabia) – Class C device submissions, PMS reporting, local regulatory compliance 🔹 UKCA / MHRA – Device registration, compliance audits 🔹 TGA (Australia) – Regulatory approvals, documentation compliance 🔹 DRAP (Pakistan) – Device registration, submissions 📌 Core Regulatory Deliverables: - Clinical Evaluation Reports (CERs) – MDR Annex XIV & MEDDEV 2.7/1 Rev.4 - Biological Evaluation Reports (BERs) – ISO 10993 series - Risk Management Files – ISO 14971:2019 - Technical Documentation – DHF, DMR, DHR, CE marking dossiers, FDA submissions - Verification & Validation Reports - Post-Market Surveillance (PMS) & PMCF Reports - Declaration of Conformity & GSPR Checklist - Labelling & Instructions for Use (IFU) 💼 Regulatory Project Experience: - Balloon stents & catheters – CER, BER, Technical File - Hypodermic needles – FDA & CE submissions - Wound management devices – PMS and technical documentation - Breast cancer detection software (SaMD) – Clinical evaluation & global regulatory strategy - IVD blood collection & DNA/RNA extraction kits – CE marking & regulatory submissions 🏆 Regulatory Experience Highlights: - Acting as PRRC, ensuring EU MDR & EUDAMED compliance for clients - Preparing, reviewing, and maintaining technical files, CERs, BERs, Risk Management Files, DHF/DMR/DHR, PMS reports - Managing global regulatory submissions across EU, FDA, SFDA, UKCA, TGA, and DRAP - Advising on device classification, intended use, borderline cases, and combination devices - Implementing and auditing Quality Management Systems in compliance with ISO 13485:2016 - Ensuring risk management and product lifecycle compliance per ISO 14971:2019 My expertise includes: • ISO 13485 Quality Management System implementation • Quality Manual preparation and documentation control • SOP (Standard Operating Procedure) development • Work Instruction creation • Form and template development • CAPA (Corrective and Preventive Action) systems • Nonconformity and deviation management • Risk Management documentation (ISO 14971) • Gap Analysis for ISO 13485 and EU MDR compliance • Internal audit preparation and audit support • Technical Documentation / Technical File preparation • Device Master Record (DMR) and Device History Record (DHR) • Change Control and Document Control systems • Supplier qualification and vendor management • Complaint handling and Post Market Surveillance (PMS) • Clinical Evaluation documentation support • Validation protocols and reports Validation Expertise: • IQ (Installation Qualification) • OQ (Operational Qualification) • PQ (Performance Qualification) • Process Validation • Equipment Validation • Cleaning Validation • Packaging Validation 🧩 Regulatory Standards & Compliance Knowledge: - ISO 13485:2016 – QMS implementation & audit readiness - ISO 14971:2019 – Risk management for medical devices - ISO 10993-1 – Biocompatibility evaluation - ISO 62366 – Usability engineering - ISO 15223-1 / ISO 20417 – Labelling & device information - IEC 60601-1 / IEC 62304 / IEC 82304-1 – Electrical & software safety - FDA 21 CFR Parts 11 & 820 – Quality system and electronic records Why Hire Me for Regulatory Affairs: ✅ Global Expertise: End-to-end RA support across EU, FDA, SFDA, UKCA, TGA, and DRAP ✅ High-Risk Device Specialist: Class III implantables, combination devices, IVDs, SaMD, borderline cases ✅ Comprehensive Documentation: CERs, BERs, Technical Files, DHF/DMR/DHR, PMS, labelling, IFU ✅ PRRC Services: Acting as your dedicated MDR compliance officer ✅ Audit-Ready & Compliant: Standards-driven, meticulous, reliable, and timely ✅ Strategic Guidance: Regulatory strategy, classification, submissions, lifecycle compliance Let’s Connect: Message me to discuss your device regulatory needs. I provide expert guidance to achieve fully compliant, market-ready, and audit-proof documentation worldwide.

🏆 100% Job Success ⭐ Top Rated Plus Freelancer Helping biotech, pharmaceutical, nutraceutical, OTC, and wellness startups transform ideas into scientifically structured, regulatory-ready products. ✅ Pharmaceutical Formulation Development, 🧬 Peptide & Injectable Product Design, 🌿 Nutraceutical & Supplement Development, 📋 FDA / EMA / OTC Regulatory Strategy, 📑 Technical Documentation & Product Dossiers, 🏭 CMC, Manufacturing & Stability Planning, 📈 Product Positioning & Scientific Branding &🔎 Research & Development Support Remote executions with CMOs/FDA / EPA / OTC / injectables / nutraceuticals

Greetings, I am an experienced Lead Auditor with 10+ years of expertise, specializing in ISO standards, including ISO 9001:2015 (QMS), ISO 14001:2015 (EMS), ISO 45001:2018 (OHSMS), ISO 22000:2018 (FSMS), ISO 27001:2022 (ISMS), ISO 13485:2016 (Medical Devices), ISO 22301:2019 (BCMS), ISO 37001:2016 (ABMS), ISO 20000-1:2018 (IT), ISO 21001:2018 (Education), ISO 50001:2018 (Energy), and ISO 41001:2018 (Facilities). I also offer certifications such as GMP, CE, FDA, Halal, Lean Six Sigma certificates, and more. We partner with various certification bodies, including ASIB, UKAS, UAF, IAS, JAS-ANZ, and IAF, and have collaborated with numerous organizations across diverse sectors to ensure compliance with these standards. If you’re looking for a versatile, detail-oriented consultant to help elevate your business, I am here to assist you. Why Choose Me: • 24/7 Availability: Always here for your support and inquiries. • Unlimited Revisions: Ensuring your complete satisfaction. • Expertise Across Sectors: Extensive experience in diverse industries. • Tailored Solutions: Customised strategies to meet your specific needs. • Proven Track Record: Successful partnerships with leading certification bodies. • Attention to Detail: Thorough and meticulous approach to audits. • Up-to-Date Knowledge: Continuous learning to stay current with ISO standards. I am ready to discuss your project and provide tailored guidance to help you find the best solutions for your business needs.