Discover now the Power of Integrated Quality Management Systems, maximizing your compliance & efficiency.
Steering Your Success with digital future-ready capabilities.
Are you ready to boost your Compliance capabilities?
Experience the Power of our ready to use QMS Solutions & Services.
Quality Management Systems Design as per National & International market regulatory requirements
Quality Policy & Quality Manual design
Ready to use SOPs, working instructions and templates
Data Integrity Strategy
Elevate QMS with Digital Transformation: Compliance meets Innovation at its best!
Converting manual quality systems to paperless eQMS - CFR Part 11 compliant
Mobile applications on QMS processes
Digital dashboards
Agile Quality Management Review
Real time quality KPIs reporting
Embrace the transformative power of our quality contract services, where each negotiation is a confident step towards your success
Negotiation strategies
Ready to use templates for all types of Quality Contracts
Digital transformation of Quality Contracts lifecycle management
Efficient metrics in contracts interactions
Streamline Your Audit Preparation
Get Ready with Expert Guidance, paving the way to seamless compliance and confidence
Baseline Assessments as per National & International health authorities requirements
Ready to use tools for audits preparation
Mock inspections
Experts coaching on hosting audits
Front and back room support
Market report on regulatory inspections trends
Don’t let your supply chain be disrupted. De-risk you supplier and service providers’ selection
Turn your supplier challenges into growth opportunities
Suppliers and Services Providers Compliance Strategies
Auditing Services
Ready to use paper audits
Risk Assessment
Suppliers Performance reviews
Ignite Learning, Elevate skills and Cultivate peoples’ growth through the power of Knowledge
Creation and delivery of technical training sessions
Workshops on real life case studies
Training events planning
Curricula design in digital format
Videos on demand
Trainers qualification programs
e-Quizzes and Polls
Satisfaction and engagement surveys
Faidra is a Pharmaceutical Process & Cleaning Validation expert with over a decade of experience in the manufacturing industry and pharmaceutical technology focusing on process optimization and process excellence. She is a Chemical Engineer by academia with Master degree in Industrial Pharmacy. She has strong scientific knowledge in all pharmaceutical dosage forms, deep understanding of Pharmaceutical Technical Operations and regulatory expectations. Her industrial experience and continuous improvement mentality, reinforce her drive to impact quality compliance and operational efficiency projects in the pharmaceutical sector.
Alexandros is a Pharmaceutical Quality Operations professional with more than 15 years΄ experience in the field of Technical Quality Assurance, Laboratory operations and Quality control systems.
He is a Chemist by academia, with a comprehensive knowledge of Pharmaceutical Quality Systems’ design, cGMPs, Compendia and industrial Guidelines, leveraging this knowledge to excel in multiple professional capacities within Manufacturing Operations and Quality Assurance. He has extensive experience in auditing, CAPAs, digital transformation, and regulatory compliance. He is also skilled in analytical methods validation and troubleshooting, data integrity, lean lab, quality risk management, and computerized system validation.
Theoni is a Pharmaceutical Quality professional with more than
17 years΄ experience in Quality Assurance, Regulatory Compliance and Laboratory Operations in various management positions, including Head of Quality Management for over 7 years.
She is a Chemist by academia and she holds a MSc in Biochemistry.
She has a strong knowledge of Quality Management Systems to EU GMP regulations, as well as Cosmetics, and has been a Qualified Person for over 14 years.
Alicia is a Pharmaceutical Quality Professional with more than 20 years’ experience in Multinational Pharmaceutical Companies for several markets (EMA, FDA, PMDA, TGA). Experienced in Quality Assurance, Quality Control and CMC from development & clinical phases to commercial stage. She is an SME in Microbiology for API & Medicinal Products (Sterile & non-sterile).
She was a graduate in Biochemistry and Molecular Biology (UAM), and after acquiring investigational background and doctorate studies (Severo Ochoa Molecular Biology Center, CBMSO), her carrier was developed in Multinational Pharma companies.
Maria is a Chemist by academia and a Pharmaceutical Quality professional with more than 18 years΄ experience in Multinational Pharmaceutical Industries in QC, QA and R&D departments.
She has a full understanding of supplier compliance regulations, with a strong knowledge of creating functional supplier management systems to cGMP regulations.
She is a Lead Supplier Auditor with over 9 years’ experience in compliance assessment standards such as EU GMP Part II, ISO 9001, ISO 17025, ISO 15378 etc.
Extensive expertise in Data Integrity aspects according to FDA and EU guidelines, with a track record of leading involvement in Data Integrity projects for over 3 years.
Anastasia is a Quality professional with more than 25 years΄ experience in Regulatory Compliance, Research and Development, Regulatory Affairs, and served as a QP for more than 15 years. She has extensive hands-on experience on developing and implementing regulatory strategies that achieve compliance with government regulations.
She is a Chemist by academia and she holds a MSc in Pharmaceutical Analysis and Quality Control.
Katerina is a Pharmaceutical Quality Operations professional with more than 25 years΄ experience in Technical Quality Assurance, Regulatory Governance and Compliance, Laboratory Operations and design of integrated Quality Management Systems.
She is a Chemist by academia with a M.Sc. in Analytical Chemistry from Northeastern University (US). Recently she acquired an Executive MBA from ALBA Graduate Business School (GR), reinforcing her drive of integrating Quality Management Systems’ design into business strategies and organizational structures.
Kiki is a Group Quality Systems expert in Pharmaceutical Industry with more than 20 years of experience in Quality Control, Quality Assurance and Inspections Management. She has a BSc degree in Biomedical Sciences and a Master Degree in Business Administrations (MBA).
Kiki has a wide knowledge on applying digital solutions on integrated quality management systems in cross functional organizations, designing and cascading strategies on people development through Training Academy programs, continuously monitoring quality systems & operations surveillance by inspections and transforming agile KPIs into OKRs, Objectives & Key Results.
Pedro is a Pharmaceutical Qualification Operations professional with more than 20 years΄ experience in Technical Areas, Engineering and Quality by design, specific to Buildings/Facility; Utilities and Equipment/Instrumentation Systems.
He is a Mechanical Engineer by training from the Engineering Institute of Lisbon, Portugal and has been working at several Pharma & Biotech companies around the Europe, as: Portugal; Ireland; UK & Netherlands, which gave him the opportunity to have a multicultural experience as well as professional.
During his first professional years, Pedro was part of the Engineering teams and at the last 6 years has been taken part of Quality departments.
Antonia is a Quality Assurance & Systems professional with over 12 years of experience and a demonstrated record of contribution on designing structural schemes of system of written procedures. She is committed and passionate about helping pharmaceutical organizations and people to meet their full potentials. She has led multi-disciplinary transformation projects, managed cross-functional and diverse teams to meet the organizational operational objectives such as operational
excellence, preventive compliance, inspection readiness, designing,
implementing and improving quality management systems.
She is a Chemist by academia and she holds a MSc in Analytical Chemistry.