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Rita Pedroso Email & Phone Number
Regulatory Affairs Manager | Tecnimede Group
at
Tecnimede Group
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✓ Verified August 2026
3 data sources
Profile completeness 100%
Current company
Role
Regulatory Affairs Manager | Tecnimede Group
Location
Lisboa, Lisbon, Portugal
Who is Rita Pedroso? Overview
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Quick answer
Rita Pedroso is listed as Regulatory Affairs Manager | Tecnimede Group at Tecnimede Group, based in Lisboa, Lisbon, Portugal. AeroLeads shows a matched LinkedIn profile for Rita Pedroso.
Rita Pedroso previously worked as Regulatory Affairs Manager at Tecnimede Group and Head of Regulatory & Scientific Affairs Department at Phagecon - Pharmaceutical Services And Consulting. Rita Pedroso holds Advanced Program In Product Management & Business Development from Invictus Sciences.
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Email format at Tecnimede Group
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Tecnimede Group
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Profile bio
About Rita Pedroso
Experienced Senior Regulatory Affairs Specialist with a demonstrated history of working in the pharmaceuticals industry. Skilled in Generic Programming, Regulatory Affairs, Quality Assurance, Pharmacovigilance, and Regulatory Requirements. Strong legal professional graduated from Universidade Lusófona de Humanidades e Tecnologias.
Listed skills include Regulatory Affairs, Regulatory Requirements, Regulatory Submissions, Generic Programming, and 4 others.
Current workplace
Rita Pedroso's current company
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12 roles
Rita Pedroso work experience
A career timeline built from the work history available for this profile.
Regulatory Affairs Manager
CurrentTeam and projects management.Experienced project manager on the following areas:- Human products: MA Applications under different types of procedures (NPs, MRPs and DCPs) in the EEA and legal basis, Variations and Renewals under the different types of procedures (NPs, MRPs, DCPs) in the different possible formats (CTD, NeeS, e-CTD, etc);- Extensive experience with the EU regulations and Guidance;- Experience on regulatory advise and strategy for the development, registration and life-cycle management for products for EU;- Experience in CMC submissions;- Quality expert reports elaboration and revision;- Extensive gap-analysis of EU dossiers for future EU submissions assuring the dossiers accuracy and compliance with the legislation in force;- IMPD constitution and submission;- Preparation, translation and revision of texts for SPC, PIL and Labelling;- Training: Internal department collaboration;- eCTD training;- Price and Reimbursement strategy and submission- Management of licensees, business partners and Competent Authorities relationships.
Feb 2021 - Present
Head Of Regulatory & Scientific Affairs Department
Phagecon - Pharmaceutical Services And Consulting
Team and projects management.Regulatory affairs consultant on the following areas:- Human and Veterinary Medicinal products: MA Applications under different types of procedures (NPs, MRPs and DCPs) in the EEA as well as Medicinal products registration in 3rd countries, e.g. outside the EEA) and legal basis, Variations and Renewals under the different types of procedures (NPs, MRPs, DCPs) in the different possible formats (CTD, NeeS, e-CTD, etc);- Extensive experience with the EU regulations and Guidance's;- Experience on regulatory advise and strategy for the development, registration and life-cycle management for products for EU - Experience in CMC submissions;- Quality expert reports elaboration and revision;- Extensive gap-analysis of EU dossiers for future EU submissions assuring the dossiers accuracy and compliance with the legislation in force;- Preparation, translation and revision of texts for SPC, PIL and Labelling;- Other Health Products life-cycle management experience (Cosmetics, biocides, medical devices and food suplements)- Importation and Exportation licences application submssion;- Training: Internal department collaboration;- External eCTD training;- Price and Reimbursement strategy and submission- Management of licensees, business partners, clients and Competent Authorities relationships.
Apr 2020 - Feb 2021
Regulatory Affairs Manager
Phagecon - Pharmaceutical Services And Consulting
Sep 2018 - Apr 2020
Regulatory Affairs Manager
Sep 2018 - Mar 2020
Senior Regulatory Affairs &Pharmacovigilance Deputy (Lso)
Tolife - Produtos Farmacêuticos, Lda.
Dec 2013 - Aug 2018
Regulatory Science Officer & Quality Assurance
Pharmaffairs Pharmaceutical Consulting Lda
Sep 2012 - Nov 2013
Regulatory Affairs Manager
Bizaffairs
Jan 2012 - Aug 2012
Regulatory Affairs Officer
Pharsolution - Pharmaceutical Consulting, Lda
Nov 2010 - Dec 2011
Regulatory Affairs
Sociedade Jneves, Lda.
Jun 2007 - Nov 2010
Technical Director
Profarin Lda
Jan 2006 - Jun 2007
Technical Director
Botelho & Rodrigues
Oct 2005 - Dec 2005
3 education records
Rita Pedroso education
Advanced Program In Product Management & Business Development
Invictus Sciences
Education record
Invictus Sciences
Pharmd, Pharmaceutical Sciences, Ciências Farmacêuticas
Universidade Lusófona - Centro Universitário Lisboa
FAQ
Frequently asked questions about Rita Pedroso
Quick answers generated from the profile data available on this page.
What company does Rita Pedroso work for?
Rita Pedroso works for Tecnimede Group.
What is Rita Pedroso's role at Tecnimede Group?
Rita Pedroso is listed as Regulatory Affairs Manager | Tecnimede Group at Tecnimede Group.
Where is Rita Pedroso based?
Rita Pedroso is based in Lisboa, Lisbon, Portugal while working with Tecnimede Group.
What companies has Rita Pedroso worked for?
Rita Pedroso has worked for Tecnimede Group, Phagecon - Pharmaceutical Services And Consulting, Ldp Laboratorios Torlan S.A., Tolife - Produtos Farmacêuticos, Lda., and Pharmaffairs Pharmaceutical Consulting Lda.
How can I contact Rita Pedroso?
You can use AeroLeads to view verified contact signals for Rita Pedroso at Tecnimede Group, including work email, phone, and LinkedIn data when available.
What schools did Rita Pedroso attend?
Rita Pedroso holds Advanced Program In Product Management & Business Development from Invictus Sciences.
What skills is Rita Pedroso known for?
Rita Pedroso is listed with skills including Regulatory Affairs, Regulatory Requirements, Regulatory Submissions, Generic Programming, Pharmacovigilance, Quality Assurance, Pharmaceutical Industry, and Generics.
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