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Barbara Szklarek Email & Phone Number
Head of Regulatory Affairs, OTC and Self-Care Market
at
PASMI Polski Związek Producentów Leków Bez Recepty
1 work email found
@wp.pl
LinkedIn matched
✓ Verified August 2026
4 data sources
Profile completeness 100%
Current company
Role
Head of Regulatory Affairs, OTC and Self-Care Market
Location
Warsaw, Mazowieckie, Poland
Company size
Who is Barbara Szklarek? Overview
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Quick answer
Barbara Szklarek is listed as Head of Regulatory Affairs, OTC and Self-Care Market at PASMI Polski Związek Producentów Leków Bez Recepty, a with 5 employees, based in Warsaw, Mazowieckie, Poland. AeroLeads shows a work email signal at wp.pl and a matched LinkedIn profile for Barbara Szklarek.
Barbara Szklarek previously worked as Chair of the Regulatory Working Group at Pasmi (Polish Association Of Self Medication Industry) and Regulatory Affairs Manager at Usp Zdrowie (Us Pharmacia). Barbara Szklarek holds Postgraduate Degree, Medical Devices Quality Management System Manager from Sgh Warsaw School Of Economics.
Company email context
Email format at PASMI Polski Związek Producentów Leków Bez Recepty
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{first_initial}{last}@wp.pl
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AeroLeads found 1 current-domain work email signal for Barbara Szklarek. Compare company email patterns before reaching out.
Profile bio
About Barbara Szklarek
Barbara Szklarek is a Head of Regulatory Affairs, OTC and Self-Care Market at PASMI Polski Związek Producentów Leków Bez Recepty. She possess expertise in regulatory affairs, regulatory submissions, pharmacovigilance, pharmaceutical industry, ectd and 9 more skills. She is proficient in English.
Listed skills include Regulatory Affairs, Regulatory Submissions, Pharmacovigilance, Pharmaceutical Industry, and 10 others.
Current workplace
Barbara Szklarek's current company
Company context helps verify the profile and gives searchers a useful next step.
Pasmi Polski Związek Producentów Leków Bez Recepty
4 roles
Barbara Szklarek work experience
A career timeline built from the work history available for this profile.
Chair Of The Regulatory Working Group
Current
Pasmi (Polish Association Of Self Medication Industry)
Nov 2021 - Present
Regulatory Affairs Manager
Current
Nov 2003 - Present
Regulatory Affairs Specialist
Feb 1996 - Oct 2003
3 education records
Barbara Szklarek education
Postgraduate Degree, Medical Devices Quality Management System Manager
Marketing/Marketing Management, General
Master'S Degree, Biotechnology
FAQ
Frequently asked questions about Barbara Szklarek
Quick answers generated from the profile data available on this page.
What company does Barbara Szklarek work for?
Barbara Szklarek works for PASMI Polski Związek Producentów Leków Bez Recepty.
What is Barbara Szklarek's role at PASMI Polski Związek Producentów Leków Bez Recepty?
Barbara Szklarek is listed as Head of Regulatory Affairs, OTC and Self-Care Market at PASMI Polski Związek Producentów Leków Bez Recepty.
What is Barbara Szklarek's email address?
AeroLeads has found 1 work email signal at @wp.pl for Barbara Szklarek at PASMI Polski Związek Producentów Leków Bez Recepty.
Where is Barbara Szklarek based?
Barbara Szklarek is based in Warsaw, Mazowieckie, Poland while working with PASMI Polski Związek Producentów Leków Bez Recepty.
What companies has Barbara Szklarek worked for?
Barbara Szklarek has worked for Pasmi Polski Związek Producentów Leków Bez Recepty, Pasmi (Polish Association Of Self Medication Industry), Usp Zdrowie (Us Pharmacia), and Aflofarm Farmacja Polska.
How can I contact Barbara Szklarek?
You can use AeroLeads to view verified contact signals for Barbara Szklarek at PASMI Polski Związek Producentów Leków Bez Recepty, including work email, phone, and LinkedIn data when available.
What schools did Barbara Szklarek attend?
Barbara Szklarek holds Postgraduate Degree, Medical Devices Quality Management System Manager from Sgh Warsaw School Of Economics.
What skills is Barbara Szklarek known for?
Barbara Szklarek is listed with skills including Regulatory Affairs, Regulatory Submissions, Pharmacovigilance, Pharmaceutical Industry, Ectd, Regulatory Requirements, Regulatory Documentation, and Ctd.
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