Hire the Best Pharmaceutical Industry Specialists
in Pakistan

I’m a Pharmacist, Regulatory Compliance Consultant & Scientific Documentation Specialist with 16+ years of experience supporting health, wellness & consumer product brands with regulatory research, compliance documentation & scientific communication. I help businesses navigate complex regulations across supplements, cosmetics, wellness products, medical devices, consumer goods & emerging healthcare categories, translating confusing regulatory requirements into clear, practical & actionable steps. Whether you’re launching a dietary supplement, reviewing cosmetic labels, assessing food contact material documentation, preparing an Amazon product listing or evaluating supplier compliance paperwork, I help ensure your products & supporting materials align with applicable regulatory expectations. My background combines pharmacy, scientific research, regulatory interpretation & technical documentation, allowing me to bridge the gap between science, compliance & business needs in a way that is accurate, strategic & easy to understand. Core Services 1. Regulatory Compliance & Product Review • Label review for dietary supplements, cosmetics, wellness products, food contact materials & consumer goods • Amazon compliance support, including CPC/CPSIA-related documentation review • Ingredient safety research & product claims assessment • Regulatory research for FDA, Health Canada, EMA, TGA, UK & international compliance frameworks • Cosmetic ingredient, packaging & labeling compliance support • Food contact material documentation review & regulatory research • Review of COAs, SDSs, test reports & supporting supplier documentation • Compliance gap analysis & risk-based documentation review • Product claims evaluation for marketing, packaging & e-commerce listings 2. Scientific & Technical Documentation • Regulatory summaries & technical documentation • SOPs, product summaries & scientific reports • Clinical & scientific literature interpretation • Evidence-based healthcare & wellness content • Medical, pharmaceutical & scientific writing • Research-backed documentation for health, wellness & consumer brands 3. Market & Product Research • Competitor & market landscape research • Product positioning & formulation trend analysis • Regulatory intelligence for global market entry • Consumer healthcare, cosmetic & supplement market research I also have experience working within highly regulated sectors including supplements, cannabinoids/CBD, pharmaceuticals, cosmetics, wellness products & emerging healthcare categories. Currently, I am expanding my expertise in product registration workflows, dossier preparation, medical device documentation support, food packaging compliance & international e-commerce compliance to better support growing global brands. Clients appreciate working with me because I combine scientific accuracy with clear communication. I understand that most founders, brand owners & e-commerce businesses are not regulatory specialists, they simply need someone dependable who can research thoroughly, communicate clearly & help them move forward with confidence. Let’s simplify compliance & build documentation that is accurate, professional & client-ready.

Hello! I'm Dr. Hina Manzoor, a PhD in Biochemistry with over 10 years of experience in the pharmaceutical industry and extensive expertise in computational drug discovery, pharmaceutical documentation, and scientific research. I have successfully worked with pharmaceutical companies, research organizations, and international clients, delivering high-quality technical and scientific solutions remotely. My background combines pharmaceutical quality systems with advanced computational biology, allowing me to provide both regulatory documentation and research-based services. My Areas of Expertise Pharmaceutical Documentation GMP/cGMP Documentation Regulatory Dossiers (CTD/eCTD) Standard Operating Procedures (SOPs) Specifications & Methods of Analysis Batch Manufacturing Records (BMRs) Validation Protocols & Reports Process & Method Validation Equipment Calibration Documents Certificates of Analysis (COAs) Stability Study Documentation CAPA, Change Control & Risk Management Documents Training Manuals and Quality Documents Policies, Protocols, Forms & Log Sheets Artwork Review (Labels, Cartons, Leaflets & Packaging Literature) Computational Drug Discovery & Bioinformatics Molecular Docking Molecular Dynamics (AMBER & GROMACS) MM/GBSA Binding Free Energy Analysis Virtual Screening Pharmacophore Modeling Structure-Based Drug Design ADMET Prediction Protein-Ligand Interaction Analysis Drug Repurposing Studies RNA/miRNA Modeling QSAR and Machine Learning for Drug Discovery Scientific Research Research Paper Writing Literature Reviews Systematic Reviews Data Analysis Publication Support Manuscript Editing Journal Formatting Figure Preparation Thesis and Dissertation Support Programming & Data Analysis Python R Programming RDKit Pandas NumPy Scikit-learn Scientific Data Analysis Automation Scripts Business & IT Solutions Excel Automation & Inventory Management Company Profiles & Presentations Custom Software Solutions Technical Documentation Web-Based Applications Ongoing Technical Support Why Work With Me? ✔ PhD in Biochemistry with specialization in Computational Drug Discovery ✔ 10+ years of pharmaceutical industry experience ✔ Published author in high-impact international journals including Scientific Reports and PLOS ONE ✔ Practical experience in pharmaceutical quality systems, regulatory documentation, and analytical method validation ✔ Experience serving international clients through Upwork ✔ Strong communication, timely delivery, and complete confidentiality Whether you need pharmaceutical documentation, scientific writing, molecular docking, molecular dynamics simulations, computational drug discovery support, Python/R-based data analysis, or regulatory documentation, I am committed to delivering accurate, professional, and high-quality work tailored to your project requirements. Feel free to contact me to discuss your project. I look forward to helping you achieve your goals.

Global Regulatory Affairs & Compliance Consultant | FDA, EMA, MHRA | Pharmaceuticals, Cosmetics, OTC & Dietary Supplements Bringing a product to market is challenging. Regulatory delays, deficient submissions, non-compliant labels, or failed audits can cost companies months of lost revenue and significant remediation expenses. I help pharmaceutical, cosmetic, OTC drug, dietary supplement, and medical device companies navigate global regulatory requirements with confidence. I am a PhD Chemist with 9+ years of Regulatory Affairs experience supporting manufacturers, brand owners, distributors, and investors across the United States, European Union, and United Kingdom. My expertise spans regulatory strategy, dossier preparation, compliance audits, market authorization, and post-approval lifecycle management. Regulatory Experience ✔ 8+ ANDAs successfully delivered ✔ 15+ EU & MHRA Hybrid Applications supported ✔ 100+ Drug Master Files (DMFs) prepared, reviewed, or remediated ✔ 18+ API compliance audits conducted in accordance with ICH Q7 ✔ 200+ cosmetic brands supported for FDA MoCRA, EU CPNP, and UK SCPN compliance ✔ 100+ OTC drug listings and NDC registrations completed ✔ 100+ dietary supplement and consumer health products launched successfully Areas of Expertise Pharmaceuticals • ANDA, IND, NDA, MAA, and Hybrid Applications • eCTD Publishing and CTD Modules 1–5 • CMC Documentation and Regulatory Strategy • Drug Master Files (DMF) • Deficiency Letter and RTR Response Support • GMP and Inspection Readiness • Regulatory Gap Assessments APIs & Excipients • ICH Q7 Compliance Audits • Supplier Qualification Programs • Quality Agreements • DMF Development and Remediation • Technical Documentation Reviews Cosmetics (US, EU & UK) • FDA MoCRA Compliance • Cosmetic Product Safety Reports (CPSR) • Product Information Files (PIF) • CPNP & SCPN Notifications • Ingredient Compliance Reviews • Labeling & Claims Compliance • Safety Data Sheets (SDS) Dietary Supplements & Consumer Health Products • FDA Compliance Reviews • Structure/Function Claim Reviews • Label Compliance • NDI Assessments • Ingredient Safety Evaluations • Facility Registration Support Medical Devices • Regulatory Strategy • Technical Documentation Reviews • FDA Registration & Listing Support • Quality System Compliance Compliance & Quality Support • GMP & GDP Compliance • Internal Audits • Supplier Audits • CAPA Systems • Change Control Programs • Risk Assessments • Regulatory Intelligence • SOP Development • Quality Management Systems Why Clients Hire Me I focus on preventing regulatory issues before they become costly business problems. Whether you need a submission-ready dossier, a compliant cosmetic launch, an FDA label review, a DMF remediation project, or an audit-ready quality system, I provide practical regulatory solutions aligned with current FDA, EMA, MHRA, and international requirements. My goal is simple: help clients achieve faster approvals, maintain compliance, and reduce regulatory risk. Let's discuss your project and identify the most efficient regulatory pathway for your product.

I am an excellent online market researcher in pharma,medical devices,consumer products.Sourcing of medical supplies,cosmetics and consumer products is my speciality.I am an experienced pharmacist with more than 10 years experience of regulatory compliance in Europe,USA,Golf and Asian countries.Medical research is my passion and can provide great results in this area.Along this I have also experience in online and physical surveys in society, markets,educational institutions and others.

I’m a licensed pharmacist (PharmD) with hands-on experience in patient counseling, medication use, and healthcare communication. I’ve worked closely with patients to help them understand their medicines, manage side effects, and use treatments safely and effectively. Over time, I’ve developed a strong interest in turning complex medical information into simple, clear, and helpful content that people can actually understand and use in real life. I specialize in writing: • Drug information and explanations • Patient-friendly health and medication guides • Medical and healthcare blog content • Antibiotic and clinical case summaries What sets me apart is that I don’t just write—I understand the medical side deeply, so the content is both accurate and practical, not just general information. I’m also open to supporting clients with: • Virtual assistant tasks (research and organization) • Beta reading for fiction (feedback on clarity, flow, and readability) Outside of work, I enjoy reading, baking, and watching series/movies—which also helps me understand storytelling and communication better.

I’m a Regulatory Affairs professional with hands-on experience in preparing export dossiers (CTD/ACTD), contract manufacturing documents, and product registrations for DRAP and international markets (Cameroon, Cambodia, etc.). I’ve worked on hormonal, antibiotic, and antiviral products, including generating CoPP, applying for renewals, and ensuring compliance with WHO, ICH, and local guidelines. Services I offer: -CTD/ACTD Dossier Compilation -DRAP Registration and Renewal Applications -Product Variation Filing -CPP Preparation Assistance -International Regulatory Research -QA/QC Documentation (if applicable)