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David Calvo is listed as Senior Regulatory Affairs Officer / Scientific background at Cloverty, based in Greater Madrid Metropolitan Area, Spain, Spain. AeroLeads shows a matched LinkedIn profile for David Calvo.
David Calvo previously worked as Senior Officer - Regulatory Dept. at Cloverty and Regulatory Officer at Laboratorios Normon. David Calvo holds Development, European Registration Procedures And Medicines Regulation, Regulatory Affairs from Colegio Oficial De Farmacéuticos De Madrid.
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PROFESSIONAL STATEMENT Responsible of Regulatory Dept. at Cloverty (head office & CDMO), accountable for Pharma and Food Supplements (FS). Activities in charge include Preparation of Registration Dossiers, Documentary + Regulatory Support, Interaction with Authorities & Customers, etc. Currently leading a team of 3 technicians providing support to +50 clients in +100 countries.Formation in Registration and Regulatory (MSc), Clinical Research and Scientific background in R&D in Pharma (GlaxoSmithKline, +10 years) with experience as Project Leader in Int’l programs.My professional objective is to progress my technical career in Regulatory, specializing in Novel Projects, Regulatory Intelligence, MAA and Cross-National Registration strategies.I provide initiative, commitment and autonomous management. KEY STRENGTHS• Excellent organizational and planning skills.• Matrix Leadership. Team Player. Accomplished communicator.• Entrepreneur – Innovative, challenging solutions: Technical / Scientific • Committed and Enthusiastic for learning. Problem solving attitude.
Listed skills include Drug Discovery, Biochemistry, Assay Development, Pharmaceutical Industry, and 27 others.
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Madrid Y Alrededores, España
Senior Regulatory Affairs Officer for Pharma products and Food Supplements.-Preparation of registration dossiers, maintenance of authorized products (i.e. variations), interaction with customers (audits, export documentation, dossier adaptation: ACTD, etc.), regulatory support and regulatory intelligence for scientific activities, etc.-Communication with.
Madrid Area, Spain
o Management of serialization project & regulatory implementation of safety features within/outside EEA for +500 medicines. Regulatory Radar and Intelligenceo Notification/maintenance of AWs. Variations: administrative, quality and safety.o Interaction with authorities, organisms and clients worldwide and evaluation of regulatory requirements
Madrid Y Alrededores, España
Project Leadership & Innovation_o Design, plan and reporting of Scientific programs. Managing of Int’l team for a Rare Genetic Condition project in collaboration with Academic Investigators (DPAc). Technical Expertise_o Contributed to the set-up of the biological assays for ca. 30 novel targets across DD phases. Generated protocols to assess toxicity.
Practice_o Identification of Microsatellites in Human tumor samples by DNA analysis.
Este curso pretende capacitar al alumno para que conozca todos los aspectos del registro de un medicamento para obtener su autorización de.
Bioavailability & Bioequivalence Module 3: Quality dossier Regulatory Officer Registration of Biotechnological Products Procedures for.
Activities and Societies: Co-founder of Sports Club at Biochemistry
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David Calvo works for Cloverty.
David Calvo is listed as Senior Regulatory Affairs Officer / Scientific background at Cloverty.
David Calvo is based in Greater Madrid Metropolitan Area, Spain, Spain while working with Cloverty.
David Calvo has worked for Cloverty, Laboratorios Normon, Glaxosmithkline, and Hospital 12 De Octubre.
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David Calvo holds Development, European Registration Procedures And Medicines Regulation, Regulatory Affairs from Colegio Oficial De Farmacéuticos De Madrid.
David Calvo is listed with skills including Drug Discovery, Biochemistry, Assay Development, Pharmaceutical Industry, Life Sciences, Biotechnology, Cell Biology, and Tutoring/Supervision Of Postgraduates On Enzyme Based Studies.
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