Eric Konan
0 SESSIONS
11+ YEARS
ARCHITECT IN RESIDENCE

Eric Konan

Director of Regulatory Affairs Department

Drug Regulatory Affairs Risk Management Pharmaceutical Compliance Leadership Project Management

Dr. Eric Konan is the Director of Regulatory Affairs at GROUPE ETHICA, managing regulatory activities for a portfolio of more than 35 pharmaceutical companies across Sub-Saharan Africa. With over 11 years of experience in the pharmaceutical industry, he has held key roles at GSK (Nairobi, Kenya) and Roche (Abidjan). Eric specializes in drug regulatory affairs, risk management, compliance, stakeholder engagement, and team leadership across diverse African markets. He holds a Doctor of Pharmacy (PharmD) from Université Félix Houphouët-Boigny and a Doctorate in Public Health from Atlantic International University. He is a Certified Scrum Master with 45+ licenses and certifications, and brings strong expertise in negotiation, advocacy, and regulatory strategy for the African pharmaceutical landscape.

LANGUAGES: fr · en
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Track Record

Professional history and operational experience

Director of Regulatory Affairs Department

2024-01 - Present

GROUPE ETHICA

Regulatory Affairs Director

2023-07 - 2023-12

GROUPE ETHICA

Regulatory Affairs Manager

2019-08 - 2023-06

GSK

Regulatory Affairs Associate

2018-02 - 2019-05

Roche

Regulatory Affairs Trainee

2017-05 - 2018-01

Roche

Regulatory Coordinator Assistant

2015-06 - 2016-07

Pharm'Afrik

Credentials

Academic background and certifications

Doctor of Pharmacy - PharmD

Pharmaceutical Sciences

Université Félix Houphouët-Boigny

2018

Doctor's Degree

Public Health

Atlantic International University

2024

Intelligence Archive

Briefings authored by this architect

Introduction aux Affaires Réglementaires Pharmaceutiques en Afrique

Introduction aux Affaires Réglementaires Pharmaceutiques en Afrique

0 students
Gestion des Variations et Renouvellements Pharmaceutiques

Gestion des Variations et Renouvellements Pharmaceutiques

0 students
Engagement des Parties Prenantes en Réglementation Pharmaceutique

Engagement des Parties Prenantes en Réglementation Pharmaceutique

0 students

Accelerator Programs

Programs led or co-facilitated by this architect

Maîtrise des Affaires Réglementaires pour l'Afrique Subsaharienne

Maîtrise des Affaires Réglementaires pour l'Afrique Subsaharienne

Lead 0 enrolled

The Vault

Resources and materials published by this architect

Checklist de Soumission CTD/eCTD pour les Marchés Africains

Checklist de Soumission CTD/eCTD pour les Marchés Africains

Document 15,000 XOF
Guide de Référence du Paysage Réglementaire Africain

Guide de Référence du Paysage Réglementaire Africain

Document 20,000 XOF