Fernanda Mendes
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Fernanda Mendes Email & Phone Number

Manager - Regularory Affairs and Pharmacovigilance at MedQuímica Indústria Farmacêutica
Location: Rio De Janeiro, Rio De Janeiro, Brazil 9 work roles 4 schools
1 work email found @actelion.com 3 phones found area 213 LinkedIn matched
4 data sources Profile completeness 100%

Contact Signals · 1 work email · 3 phones

Work email f****@actelion.com
Direct phone (213) ***-****
LinkedIn Profile matched
3 free lookups remaining · No credit card
Role
Manager - Regularory Affairs and Pharmacovigilance
Location
Rio De Janeiro, Rio De Janeiro, Brazil
Company size

Who is Fernanda Mendes? Overview

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Quick answer

Fernanda Mendes is listed as Manager - Regularory Affairs and Pharmacovigilance at MedQuímica Indústria Farmacêutica, a company with 527 employees, based in Rio De Janeiro, Rio De Janeiro, Brazil. AeroLeads shows a work email signal at actelion.com, phone signal with area code 213, and a matched LinkedIn profile for Fernanda Mendes.

Fernanda Mendes previously worked as Manager - Regularory Affairs and PV at Medquímica Indústria Farmacêutica and Regulatory, Quality and Pharmacovigilance Latin America Head at Laboratoires Théa. Fernanda Mendes holds Postgraduate Studies, Industrial Pharmacy from Estácio.

Company email context

Email format at MedQuímica Indústria Farmacêutica

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{first}.{last}@actelion.com
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AeroLeads found 1 current-domain work email signal for Fernanda Mendes. Compare company email patterns before reaching out.

Profile bio

About Fernanda Mendes

• Bachelor’s Degree in Pharmacy• Postgraduate in Public Health and Industrial Pharmacy• MBA in Marketing Management• Career developed in national and multinational industries in the Regulatory / Compliance / Pharmacovigilance / Access area• Team Management and Development• Monitoring of processes with ANVISA, Renewal of licenses, Control of Trademark Registration with INPI, new licenses, price registration with CMED, submission of incorporation protocol to PCDT, submission of pharmacovigilance reports, document reconciliation, access to the public and private sector• Planning and launching products with the Marketing area• Coordination and planning of international inspections (Germany, England, Mexico, Argentina, USA, Italy and Japan)• Request and monitoring of drug prices with CMED• Implementation of the Pharmacovigilance sector together with the medical area• Preparation of Pharmacoeconomics reports• Quality control of pharmaceutical products• Responsible for the quality assurance / control area• Management of the compliance and training area• Monitoring and submission of products to the Ministry of Health• Performance in Government Affairs• Experienced in submitting drugs for Rare Diseases• SAP user• Fluent English

Listed skills include Sistema De Qualidade, Clinical Trials, Biotecnologia, Gmp, and 20 others.

Current workplace

Fernanda Mendes's current company

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MedQuímica Indústria Farmacêutica
Medquímica Indústria Farmacêutica
Manager - Regularory Affairs and Pharmacovigilance
Rio De Janeiro, Rio De Janeiro, Brazil
Website
Employees
527
AeroLeads page
9 roles

Fernanda Mendes work experience

A career timeline built from the work history available for this profile.

Regulatory, Quality And Pharmacovigilance Latin America Head

Nov 2020 - Dec 2022

Regulatory Affairs Head

  • Pharmaceutical Legislation
  • Registration of new and generic products, monitoring them with ANVISA. Specifically medicines that treat rare diseases
  • Analysis of regulatory non-conformities ASO and responsable for SAC.
  • Management of the operation of the Quality Control Laboratory - Quality Management. Quality system and procedures. Deviations and standards
  • Management of the quality assurance and compliance area
  • Responsible Pharmacist
Jan 2017 - Jun 2020

Regulatory Affairs Director, Compliance And Quality Champion

Rio De Janeiro, Brasil

  • Pharmaceutical Legislation
  • Registration of new and generic products, monitoring them with ANVISA. Specifically medicines that treat rare diseases
  • Analysis of regulatory non-conformities ASO and responsable for SAC.
  • Management of the operation of the Quality Control Laboratory - Quality Management. Quality system and procedures. Deviations and standards
  • Management of the quality assurance and compliance area
  • Responsible Pharmacist and Affiliate Safety Officer (ASO)
Apr 2009 - Jan 2017

Senior Manager Regulatory Affairs

  • Pharmaceutical Legislation
  • Protocol for balances of psychoactive substances and processes related to drugs, food, health products and cosmetics and monitoring them with ANVISA
  • Product registration and follow-up with ANVISA
  • International inspections
  • Product registration with Abbott International affiliates
  • Support for Quality Assurance in opening reports of non-conformities and deviations
Mar 2008 - Apr 2009

Regulatory Affairs Manager

Rio De Janeiro Area, Brazil

  • Pharmaceutical Legislation
  • Product registration and follow-up with ANVISA
  • Psychoactive substances balance sheets and processes related to medicines and cosmetics and their monitoring with ANVISA
  • Analysis of regulatory non-conformities
  • International inspections
  • Correction of final artwork and promotional materials
Jul 2007 - Feb 2008

Regulatory Affaris Coordinator

  • Pharmaceutical Legislation
  • Balance sheets for psychoactive substances and processes related to drugs, cosmetics, herbal medicines, health products and food; follow-up with ANVISA
  • Analysis of regulatory non-conformities.
  • Request and monitoring of drug prices with CMED
  • International inspections in compliance with RDC No. 25/99. Support for quality assurance in procedures and ISO audit
  • Implementation of the Pharmacovigilance sector together with the medical area
Feb 2003 - Jul 2007

Regulatory Affairs Analyst

Rio De Janeiro Area, Brazil

  • Monitoring of Pharmaceutical Legislation in order to minimize regulatory impacts in different areas of the company
  • Balance sheets for psychoactive substances and processes related to drugs; follow-up with ANVISA
  • Request and monitoring of drug prices with CMED
  • International inspections.
  • Correction of final artwork and promotional materials
  • Control authorizations and renewals
Feb 1999 - Mar 2003
4 education records

Fernanda Mendes education

Postgraduate Studies, Industrial Pharmacy

Postgraduate Studies, Public Health

Bachelor’S Degree, Pharmacy

Universidade Federal Do Rio De Janeiro

Master Of Business Administration - Mba, Marketing Management

Universidade Federal Do Rio De Janeiro
FAQ

Frequently asked questions about Fernanda Mendes

Quick answers generated from the profile data available on this page.

What company does Fernanda Mendes work for?

Fernanda Mendes works for MedQuímica Indústria Farmacêutica.

What is Fernanda Mendes's role at MedQuímica Indústria Farmacêutica?

Fernanda Mendes is listed as Manager - Regularory Affairs and Pharmacovigilance at MedQuímica Indústria Farmacêutica.

What is Fernanda Mendes's email address?

AeroLeads has found 1 work email signal at @actelion.com for Fernanda Mendes at MedQuímica Indústria Farmacêutica.

What is Fernanda Mendes's phone number?

AeroLeads has found 3 phone signal(s) with area code 213 for Fernanda Mendes at MedQuímica Indústria Farmacêutica.

Where is Fernanda Mendes based?

Fernanda Mendes is based in Rio De Janeiro, Rio De Janeiro, Brazil while working with MedQuímica Indústria Farmacêutica.

What companies has Fernanda Mendes worked for?

Fernanda Mendes has worked for Medquímica Indústria Farmacêutica, Laboratoires Théa, The Janssen Pharmaceutical Companies Of Johnson & Johnson, Actelion (Now Janssen Pulmonary Hypertension), and Abbott.

How can I contact Fernanda Mendes?

You can use AeroLeads to view verified contact signals for Fernanda Mendes at MedQuímica Indústria Farmacêutica, including work email, phone, and LinkedIn data when available.

What schools did Fernanda Mendes attend?

Fernanda Mendes holds Postgraduate Studies, Industrial Pharmacy from Estácio.

What skills is Fernanda Mendes known for?

Fernanda Mendes is listed with skills including Sistema De Qualidade, Clinical Trials, Biotecnologia, Gmp, Ectd, Requisitos Regulamentares, Regulatory, and Regulatory Affairs.

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