Sarpharma
S.A.R. Pharma S.r.l., founded in 2019, is a trusted partner for companies in the pharmaceutical, nutraceutical, cosmetic, medical, and healthcare sectors. The company offers specialized consulting in Regulatory Affairs, Pharmacovigilance, Quality, and Research & Development, ensuring compliance with high regulatory standards through strategic, innovative, and customized solutions. With over 10 years of experience, S.A.R. Pharma supports clients in navigating complex regulatory landscapes, conducting audits, inspections, and compliance strategies to ensure safety, reliability, and global success. The company's core values include Integrity, Excellence, Innovation, and Collaboration, guiding its commitment to building valuable partnerships and delivering tangible results.
Industries
Nr. of Employees
small (1-50)
Products
Dietary supplement formulations (women's health, detox, weight management)
Formulated oral supplements targeting menopause support, detoxification and weight management; developed with evidence-based ingredient selection and designed for optimized absorption and safety.
Cosmetic formulations (anti‑age creams, serums)
Topical cosmetic products formulated with active ingredients such as peptides and hyaluronic acid, developed for stability, safety and regulatory compliance.
Medical device prototypes and diagnostic instruments
Design and prototyping support for medical devices and diagnostic tools, including integration of smart technologies and compliance-focused development.
Laboratory diagnostic instruments and testing tools
Selection and advisory on laboratory instruments for analysis and health monitoring, intended to support analytical testing and product quality verification.
Dietary supplement formulations (women's health, detox, weight management)
Formulated oral supplements targeting menopause support, detoxification and weight management; developed with evidence-based ingredient selection and designed for optimized absorption and safety.
Cosmetic formulations (anti‑age creams, serums)
Topical cosmetic products formulated with active ingredients such as peptides and hyaluronic acid, developed for stability, safety and regulatory compliance.
Medical device prototypes and diagnostic instruments
Design and prototyping support for medical devices and diagnostic tools, including integration of smart technologies and compliance-focused development.
Laboratory diagnostic instruments and testing tools
Selection and advisory on laboratory instruments for analysis and health monitoring, intended to support analytical testing and product quality verification.
Services
Consulting for product registration, authorization, variations, renewals and market access strategy across medicines, medical devices, supplements and cosmetics.
Design and operation of safety monitoring systems, adverse event reporting, signal management and risk minimization for marketed products.
Implementation and optimization of Quality Management Systems, internal and external audit support, certification assistance (ISO, GMP/GDP/GVP) and documentation management.
Scientific and operational R&D support including formulation design, delivery system development, product development pathways and launch planning.
Preparation for regulatory inspections and audits, gap analysis, mock inspections and corrective action planning to achieve compliance with GMP/GDP/GVP and ISO standards.
Consulting for product registration, authorization, variations, renewals and market access strategy across medicines, medical devices, supplements and cosmetics.
Design and operation of safety monitoring systems, adverse event reporting, signal management and risk minimization for marketed products.
Implementation and optimization of Quality Management Systems, internal and external audit support, certification assistance (ISO, GMP/GDP/GVP) and documentation management.
Scientific and operational R&D support including formulation design, delivery system development, product development pathways and launch planning.
Preparation for regulatory inspections and audits, gap analysis, mock inspections and corrective action planning to achieve compliance with GMP/GDP/GVP and ISO standards.
Expertise Areas
- Regulatory affairs management
- Pharmacovigilance and safety surveillance
- Quality management and compliance (QMS)
- Research & development for pharmaceuticals, nutraceuticals and cosmetics
Key Technologies
- Quality Management Systems (QMS)
- GMP/GDP/GVP compliance
- ISO 9001-based management
- Pharmacovigilance databases and signal detection
News & Updates
Pharmacovigilance is essential for monitoring the safety of medicinal products post-marketing, involving activities like data collection, signal detection, and risk assessment to ensure patient safety.
Regulatory affairs focus on ensuring product compliance with regulations and laws, involving documentation, communication with authorities, and strategic planning to facilitate product approval and market access.
Quality assurance involves establishing and maintaining quality management systems to ensure products meet standards throughout their lifecycle, from research to post-marketing activities.
Pharmacovigilance is essential for monitoring the safety of medicinal products post-marketing, involving activities like data collection, signal detection, and risk assessment to ensure patient safety.
Regulatory affairs focus on ensuring product compliance with regulations and laws, involving documentation, communication with authorities, and strategic planning to facilitate product approval and market access.
Quality assurance involves establishing and maintaining quality management systems to ensure products meet standards throughout their lifecycle, from research to post-marketing activities.