News & Events
- News
- Webinars
- Events
Resource Library
Careers
Training

Top Bar

MENUMENU

About UsAbout Us
Our Services
- Discovery / Non-clinical
  - - - Go to Discovery / Non-clinical section >>
  - - - Strategy and Consulting
        Development Strategy and Gap Analysis
        Integrated Product Development
        Market Access Strategy
        Non-clinical Development Concept
        and Study Design
        Scientific Advice
        Scientific Due Diligence
        Statistical Services
        Toxicology Services
- Clinical Development
  - - - Go to Clinical Development section >>
  - - - Strategy and Consulting
        Clinical Program Development
        Orphan Drug Designation
        Pediatric Investigation Plan (PIP)
        Scientific Advice
        Statistical Services
      - Regulatory Affairs
        Clinical Trial Applications (CTA)
        Global Procedure Management
        Health Authority / Agency Interaction
    - - Pharmacovigilance
        Clinical Trial Safety Support
        Pharmacovigilance Consulting
      - Quality
        GxP Services
        IMP Management
        Interim / Contract QA
        Quality Systems
        Tech Transfer / Scale-up
        Vendor Management and Oversight
- Authorization / Approval
  - - - Go to Authorization / Approval section >>
  - - - Strategy and Consulting
        Market Access
      - Regulatory Affairs
        CMC Services
        Global Procedure Management
        Health Authority / Agency Interaction
        Marketing and Labeling Activities
        Scientific, Regulatory and Technical Writing
        Statistical Services
    - - Pharmacovigilance
        EU QPPV / National QPPV
        Pharmacovigilance Consulting
        Risk Management Support
      - Quality
        Commercialization Readiness
        Commissioning, Qualification, and Validation (CQV)
        GxP Services
        Interim / Contract QA
        PAI Readiness
- Post-approval / Maintenance
  - - - Go to Post-approval / Maintenance section >>
  - - - Strategy and Consulting
        Environmental Risk Assessment
        Market Access
      - Regulatory Affairs
        CMC Services
        Global End-to-End Outsourcing
        Global Procedure Management
        Health Authority / Agency Interaction
        Marketing and Labeling Activities
        Mergers and Acquisitions (M&A) Transfers
        Toxicology Services
      - Pharmacovigilance
        Audit and CAPA Management
        EU QPPV / National QPPV
        ICSR Management
        Literature Screening
        Pharmacovigilance Systems
        Safety Writing (PSUR, RMP)
        Signal Management
    - - Quality
        Commissioning, Qualification, and Validation (CQV)
        Good Distribution Practice (GDP) Compliance
        GxP Services
        Interim / Contract QA
        Quality Systems
        Vendor Audit
        Vendor Management and Oversight
      - Medical Affairs
        Healthcare Compliance and Medical Approval
        Medical Information
- Program Management
  - - - Go to Program Management section >>
      - Program Management
        Global End-to-End Outsourcing
        Global Procedure Management
        Integrated Product Development
        Mergers and Acquisitions (M&A) Transfers
- Featured Expertise
  - - - Industry Expertise
        Biopharmaceuticals
        Consulting
        Consumer Healthcare
        Generics
        Herbal Medicines
        Medicinal Products
        MedTech Services
        Pharmaceutical
        Veterinary Drugs
    - - Service Expertise
        ATMP / Cell and Gene Therapy
        Brexit
        COVID-19 Support
        Drug Re-purposing / Value-added Medicines
        GxP Services
        Market Access
        Pharmacoepidemiology
        Statistical Services
        Supporting Rx to OTC switches
      - SMARTPHLEX - technology-enabled services
Global ReachGlobal Reach
Contact usContact us
News & Events
Resource Library
Careers
Training

Home > News & Events > Event

Events

TOPRA Symposium 2020

October 5 - 7th, 2020
Visit us at booth #37

Society of Quality Assurance (SQA) Virtual Meeting and Quality College 2020

September 21 - 29th, 2020

Forum Institut für Management: eSubmissions – Ihre To-dos 2021

November 23 - August 24th, 2020

KENX Validation and GMP University

August 24 - July 26th, 2020
03:00 PM CET

KENX Risk-Based Supply Chain Validation & Verification

July 16th, 2020

DIA Europe 2020

June 30 - July 3rd, 2020
Visit us at booth #J4/K4

How to Choose the Best Quality and Regulatory Consultants

- January 24th, 2020

CPhI Worldwide 2019

November 5 - 7th, 2019
Visit us at booth #120D40

PDA / FDA Joint Regulatory Conference

November 5 - 7th, 2019
Visit us at booth #120D40

ISPE Boston Product Show

November 5 - 7th, 2019
Visit us at booth #120D40

1 2 3 4 5

prev next

Upcoming Webinars

November 26th, 2020

Software Suite for the Lifecycle of Analytical Methods & Bioassays: Gain Trust in your Results

4PM CET

December 1st, 2020

Excipient Risk Assessment as per the EU Guidance and SMARTRISK as a solution

3PM CET

December 3rd, 2020

Eudravigilance: overcoming challenges and gaining efficiencies with SMARTVIGISCREEN

3 PM CET

Archive

USEFUL LINKS

Home
Contact us
Imprint
Data Protection
Terms and Conditions

RECENT TWEETS

Tweets by @PharmaLexGLOBAL

COVID-19 NEWSLETTER SIGN UP

WHAT OUR CLIENTS SAY

Pharmalex provided the resources we needed to compile Investigational Medicinal Product Dossiers for our biological products. The dossiers were delivered on time with the trusted quality we expected

Small US Biopharmaceutical Company
Sr Director Regulatory Affairs CMC

ISO9001:2015 Logo

#AskTheExpert #TogetherBEYONDCOVID19

Select your state:

Please tick this box to agree to our Privacy Policy

Please tick this box if you agree to periodic updates from PharmaLex.
You can unsubscribe at any time at data.protection@pharmalex.com

Please leave this field empty.

If you do not wish to receive any communication from us, you can unsubscribe at any time at. Click here to view our Privacy Policy.

#TogetherBEYONDCOVID19

We closely monitor developments and updates surrounding the current outbreak of Coronavirus Disease 2019 (COVID-19) from official sources including the World Health Organisation and are following the guidance and direction of the governments and the local authorities. We are taking this situation very seriously and our number one priority is the safety and business continuity for our customers and colleagues. As ever, we will do everything we can to ensure that services are delivered within the required time and the trusted quality PharmaLex is known for

Please DO NOT send us event/conference information.
We will not respond and these will be deleted immediately.

Select your state:

Please tick this box to agree to our Privacy Policy

Please tick this box if you agree to periodic updates from PharmaLex.
You can unsubscribe at any time at data.protection@pharmalex.com

Please leave this field empty.

If you do not wish to receive any communication from us, you can unsubscribe at any time at. Click here to view our Privacy Policy.

This can be specific information about signing up to the newsletter.

Pellentesque lobortis, tellus at ultrices ullamcorper, lectus tellus consectetur lectus, id consequat leo quam quis eros. Mauris pellentesque tortor a augue pellentesque ultricies. Phasellus sit amet suscipit orci, vel dapibus ligula. Maecenas at pellentesque lectus, sit amet tristique felis. Integer fringilla risus ac neque mollis, at imperdiet lacus sodales. In vehicula orci sed vulputate interdum. Nunc sagittis non nunc eget sollicitudin.

Maecenas a mattis erat. Phasellus cursus erat non nisl pulvinar ultricies. Aenean id fringilla libero. Orci varius natoque penatibus et magnis dis parturient montes, nascetur ridiculus mus. Morbi in ultrices elit. Suspendisse egestas hendrerit est. Integer pellentesque nisl ut justo tempus, nec suscipit dolor luctus. Cras vestibulum elementum tincidunt.

In compliance with the Spanish Law 15/1999, of Protection of Personal Data and in accordance with regulations approved by the Spanish RD 994/1999 inform you that your data will be part of a file located in Friedrichsdorf (Germany), whose ownership belongs to Pharmalex Spain S.L.U. The purpose of these data is the insertion in a potential job selection process. Inform the user that at any time may exercise their right of access, rectification, and deletion of data through email curriculum@pharmalex.com or to this postal address Pharmalex Spain. Coso 103, 50001 Zaragoza, Spain.

Strategy and Consulting

Strategy and Consulting

Regulatory Affairs

Pharmacovigilance

Quality

Strategy and Consulting

Regulatory Affairs

Pharmacovigilance

Quality

Strategy and Consulting

Regulatory Affairs

Pharmacovigilance

Quality

Medical Affairs

Program Management

Industry Expertise

Service Expertise

TOPRA Symposium 2020

Society of Quality Assurance (SQA) Virtual Meeting and Quality College 2020

Biotech Atelier

Forum Institut für Management: eSubmissions – Ihre To-dos 2021

KENX Validation and GMP University

KENX Risk-Based Supply Chain Validation & Verification

DIA Europe 2020

DIA RSIDM 2020

How to Choose the Best Quality and Regulatory Consultants

CPhI Worldwide 2019

PDA / FDA Joint Regulatory Conference

ISPE Boston Product Show