Your registration is binding. The General Terms of Business enter into effect as soon as we accept your registration. Upon registration an invoice will be sent to you. Registration will be considered complete upon receipt of your payment.
We may not be able to execute the event as planned due to force majeure or due to other serious incidents.
In such case, we will offer an alternative date, as far as possible. You may book this alternative date free of charges.
In case Famar cancels the event for any reason other than force majeure or serious incident you are only entitled to the refund of the participation fees already paid; further claims are explicitly excluded. Reimbursement is carried out using the same means of payment as you used for paying the registration fee. Refunds will be made to the persons who affected the payment to us
If you want to cancel your participation for any reason we are not responsible for, you have to do so in writing and have the right to name a substitute participant to the booked registration to replace you. In case of such cancellation you are not entitled to any refund or other reimbursement.
If necessary, and in order to preserve the key aspects of the event as outlined, we may modify certain elements of the event. In such cases, if the change is minor for participants given the specific circumstances, you will not be entitled to a price reduction or a refund.
The contents represent the opinions of the individual speakers or course creators without legal guarantee. Video / Audio recording during the event is strictly prohibited. The participant(s) are prohibited from copying, recording, reproducing, distributing, publishing, displaying, transmitting, or otherwise exploiting any such content. Additionally, they may not distribute any portion of the event content over any network, including a local area network, sell or offer it for sale, or use the content to create any type of database.
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.
