We are a life sciences global industrial and quality consulting firm specializing in quality compliance and audits.​At HALTYS PM, we understand that quality assurance is essential in ensuring that pharmaceutical products and medical devices are safe and effective for patients.Life sciences global industrial and quality consulting 'Project Management, Operations, Quality Compliance and Audits'.Standards and regulations: EU Vol. 4, EU GMP/GDP, 21 CFR part 210/211/820, ICH Q7/Q9, IPEC Excipient GMPs/GDP, ISO13485, ISO 22716, ISO 17025, ISO 22000, HACCP, ISO 9001, Drug Nitrosamines risk analyzes etc.Varied experiences in the following companies: Lonza Cell & Gene Therapy Netherlands - Merial France - Sanofi Pasteur France - Octapharma France - Assistance Publique Hôpitaux de Paris France - SQA Services US (Pfizer - Merck - Baxter) - SpineSave AG Switzerland - Blanco Medical Germany - Swiss Medtech Switzerland - Laboratoires Sicobel France - Martin Dow Pharmaceuticals France - Innothera France - VEEVA Systems Vault.In various specialties: Cell and Gene Therapy - Human and Veterinary Vaccines - Human Blood - Rares Diseases - Generic Drug - Spine Implant - Medical Furniture - Dermocosmetics - CSV Computer System Validation.We have a series of services including: - Quality Assurance Operations & Systems, Compliance- Quality Project Management- Pharma, CDMO and Biologics Technology Transfer- Suppliers and Subcontractors Qualification and Management- Internal and External Audits, EU and FDA Inspections Readiness- GxP Computerized System Validation- Good Distribution Practices (GDP)- French headquarters Quality Assurance "QA Exploitant"