🎥 Step inside our GMP production facility in Antwerp. Take the 360° tour. ✳️ Class B, C, D cleanrooms ✳️ Real-time environmental monitoring ✳️ In-house QPs and 10+ trial pharmacists ✳️ 100m from our clinical unit Designed and built for risk control, speed and flexibility. Ready for your next trial. 👇 Take the virtual tour. You can find our production facility on the 1st floor. https://bit.ly/3X9CaFe #clinicalresearch #facilitytour
SGS Pharma
Pharmaceutical Manufacturing
Geneva, - 21,743 followers
Health Inspired, Quality Driven.
About us
Optimize your medicines and medical device development to get to the market safely and quickly, utilizing SGS Pharma's unique expertise, resources, and network. Contact us: pharma@sgs.com ---- We are SGS – the world's leading testing, inspection, and certification company. We are recognized as the global benchmark for sustainability, quality, and integrity. Our 99,600 employees operate a network of 2,600 offices and laboratories. --- Intellectual Property Statement: Except where expressly stated otherwise, all intellectual property rights, including copyright and trademarks, in any and all communications and materials in any form published by or on behalf of SGS are owned by SGS Société Générale de Surveillance SA, Switzerland. Link to statement on sgs.com: https://www.sgs.com/en/intellectual-property-statement
- Website
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https://www.sgs.com/en-gb/our-services/health-and-nutrition/pharma
External link for SGS Pharma
- Industry
- Pharmaceutical Manufacturing
- Company size
- 10,001+ employees
- Headquarters
- Geneva, -
- Founded
- 1878
- Specialties
- Analytical laboratory testing, Clinical Research, Biosafety testing, Quality Control testing, Contract Research Organization, Biologics cell line characterization, Biometrics services, Phase 1 clinical trials, Phase 2 clinical trials, Bioanalysis, Virology, Clinical trials Modeling and Simulation, Biosimilar testing, Extractables & Leachables studies, Data Management, Drug Development consultancy, Pharmacovigilance and Drug Safety, Method Development and Validation, Stability studies, Utilities testing and Monitoring, Elemental Impurities testing, Life Sciences, CRO, Biosafety, Human Viral challenge testing, and CDMO
Updates
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Hear Nick Praet explain how challenge agents can help you see efficacy signals for your IMP sooner, which models are commonly used and why this approach is gaining traction in early phase design. 📆 December 4 | 3PM CET 👉 Register here https://bit.ly/47HwRSe #clinicalresearch #pharma #biotech
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💡 Explore this issue of the SGS Pharma Bulletin. 👇 In this edition: ✅ how to de-risk development with standardized antibiotic potency testing ✅ how to turn phase I regulatory feedback into sharper study designs ✅ how Belgium’s ecosystem can help you shorten early-phase trials timelines ✅ how to keep biosimilar programs compliant and on schedule #pharma #clinicalresearch #drugdevelopment #biotech
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ICH E6 R3 is all about a mindset shift. The question is: can you demonstrate proportionality, training and oversight? Our latest article shares 3 practical steps to boost post-R3 confidence. Read here 👉 http://bit.ly/4oJDDhd #clinicalresearch #GCP
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Quality isn’t a destination, but it’s a daily mindset. On World Quality Day, our teams took that idea literally with a treasure hunt game across our offices, focused on quality know-how. A playful reminder on key principles like ICH GCP, data governance and good documentation practice. Because when quality becomes a shared adventure, awareness sticks. #clinicalresearch #worldqualityday
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The FDA conducted an unannounced inspection at our clinical pharmacology unit, reviewing a completed pivotal bioequivalence study and our processes end to end. And… no reported findings. This outcome is a testament to the deep-rooted quality culture and operational excellence that guide our work every day. It reflects who we are: meticulous, transparent and fully committed to delivering high-quality clinical research. 👏 Congratulations to our exceptional team! #clinicalresearch #FDA #operationalexcellence #WorldQualityDay
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Webinar: USP 665 – expert insights from USP and SGS USP 665 becomes mandatory in May 2026. Join our free webinar to hear directly from USP and SGS experts on how to prepare for E&L compliance, understand regulatory expectations and address common industry challenges. When: November 20, 2025, at 2:00 PM GMT Register now: https://lnkd.in/eWVXATz8 #drugdevelopment #pharma #biopharma #USP665 #extractables #leachables
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💪 When you need to be sure – choose SGS for your clinical research. From data collection to submission, our biometric experts turn complexity into clarity. Through initiatives like CDISC Open Rules, we’re helping the industry set new standards for data quality and transparency. #clinicalresearch #pharma #innovation #PHUSE
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Developing peptide or protein therapeutics? SGS helps you accelerate development, de-risk analytics and meet global regulatory expectations. With over 40 years of laboratory experience, we deliver comprehensive structural, functional and stability testing—giving you the data to make faster, safer decisions. Read the technical factsheet 👇 #drugdevelopment #biotherapeutics #peptides #proteins
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Small batches, unstable formulations, last-minute changes? This is phase I clinical research. And it’s exactly what our GMP production facility was built for. ✔️ On-site production ✔️ Adaptive protocols ✔️ Real-time QP support Explore our services 👇 More info: clinicalresearch@sgs.com #clinicalresearch #GMP #IMP #earlyphase