Skip to content
+31 (0) 629075858Aristotelesstraat 16, 1064 LD, AmsterdamBulevardul Unirii 11, Bloc 2B, Sector 4, Bucharest
Linkedin page opens in new window
RegPakBiopharma
RegPak BioPharma Consulting (“RegPak”) is a full-service consulting company based in Amsterdam and Romania. We offer a wide range of services in advisory, technical and administrative aspects to BioPharma, Medical Device and Nutraceutical Companies. We support our customers and their vendors, suppliers, and service providers to conduct their business both within regulatory compliance and with reduced risk. Accurately assessing and tailoring the needs of each project to individual client requirements. By working as a team, each stage of the project focuses on shortening the final timeline.
RegPakBiopharmaRegPakBiopharma

Schedule an introductory call today!
+31 (0) 629075858

  • About
  • Resources
  • Our Services
    • Menu iconAll Services
    • Menu iconDiscovery / Non-clinical
      • Strategy and Consulting
        • Non-clinical Development Concept
        • Study Design
        • Scientific Due Diligence
    • Menu iconClinical Development
      • Strategy and Consulting
        • Clinical Program Development
        • Statistical Services
        • Medical Device
      • Regulatory Affairs
        • Clinical Trial Applications (CTA)
        • CE Marking
        • Orphan Drug Designation
        • Pediatric Investigation Plan (PIP)
        • Scientific Advice
        • Early Access/Compassionate Use
      • Pharmacovigilance
        • Clinical Trial Safety Support
        • Pharmacovigilance Consulting
        • Medical Devices Vigilance
      • Quality
        • GxP Services
        • Interim / Contract QA
        • Quality Systems
        • Vendor Management and Oversight
        • ISO Compliance for medical devices
      • Clinical Trial Service
        • Site Selection & Clinical Trial Monitoring
        • Clinical Trial Documentation Authoring
        • Clinical Project Management
        • Independent Data Safety Monitoring Committee
    • Menu iconProduct Authorization / Market Approval
      • Strategy and Consulting
        • Market Access
        • Global Procedure Management
        • Medical Device
      • Pharmacovigilance
        • EU QPPV / National QPPV
        • Literature monitoring
        • Risk Management Support
        • Audit and CAPA Management
        • Medical devices Vigilance
      • Regulatory Affairs
        • CMC Services
        • Health Authority / Agency Interaction
        • Marketing Authorization and Labeling Activities
        • Scientific, Regulatory and Technical Writing
        • Environmental Risk Assessment
        • Leaflet readability testing
      • Quality
        • Commercialization Readiness
        • GxP Services
        • Interim / Contract QA
        • QP Services
      • Medical devices
        • Clinical Evaluation
        • Clinical and Safety Evaluation
        • ISO 13285 QMS
        • Notified Body Interactions
        • Authorized EU Representative
    • Menu iconPost-approval / Maintenance
      • Strategy and Consulting
        • Market Access
        • Medical Device
      • Regulatory Affairs
        • CMC Services
        • Global Procedure Management
        • Health Authority / Agency Interaction
        • Marketing and Labeling Activities
        • Post Approval Commitments and Variations
      • Pharmacovigilance
        • Audit and CAPA Management
        • EU QPPV / National QPPV
        • ICSR Management
        • Literature Screening
        • Pharmacovigilance Set-up
        • Safety Writing
        • Signal Management
        • Medical devices Vigilance
      • Quality
        • GxP Services/Audits
        • Interim / Contract QA
        • QMS Set-up
        • Vendor Management and Oversight
        • Medical device compliance
      • Medical Affairs
        • Medical Information
        • Promotional Material Review
  • Customized
    • Product Expertise
      • Cosmeceutical
      • Small Molecules
      • Biologics
      • Cell, Gene and Tissue Therapies
      • Biosimilar/Follow-on Biologics
      • Medical Devices
      • Drug-Device Combinations
      • In Vitro Diagnostics
      • Companion Diagnostics
      • Foods and Nutraceuticals
      • Vaccines
    • Therapeutic Areas
      • Oncology
      • CNS
      • Infectious Diseases
      • Hematology
      • Autoimmune System
      • Cardiovascular Disease
      • Gastrointestinal
      • Metabolic Disorder
      • Ophthalmology
      • Dermatology
    • Industry Expertise
      • Biopharmaceuticals
      • BioTech Products
      • Biosimilars
      • Consumer Healthcare
      • Genetics
      • Herbal Medicines
      • Vaccines
      • Gene Therapy
      • Small Molecules
      • Medical Device
      • Health Supplements
    • Service Expertise
      • Clinical Trial Support
      • Regulatory Affairs
      • Pharmacovigilance
      • Medical Writing
      • EU Batch Release & Testing
      • Parallel Import
      • Distribution & Supply Chain Support
      • Quality Assurance
      • Early Access/Compassionate Use
      • Orphan Drug Development
  • Contact
Search:
SEARCH
  • About
  • Resources
  • Our Services
    • Menu iconAll Services
    • Menu iconDiscovery / Non-clinical
      • Strategy and Consulting
        • Non-clinical Development Concept
        • Study Design
        • Scientific Due Diligence
    • Menu iconClinical Development
      • Strategy and Consulting
        • Clinical Program Development
        • Statistical Services
        • Medical Device
      • Regulatory Affairs
        • Clinical Trial Applications (CTA)
        • CE Marking
        • Orphan Drug Designation
        • Pediatric Investigation Plan (PIP)
        • Scientific Advice
        • Early Access/Compassionate Use
      • Pharmacovigilance
        • Clinical Trial Safety Support
        • Pharmacovigilance Consulting
        • Medical Devices Vigilance
      • Quality
        • GxP Services
        • Interim / Contract QA
        • Quality Systems
        • Vendor Management and Oversight
        • ISO Compliance for medical devices
      • Clinical Trial Service
        • Site Selection & Clinical Trial Monitoring
        • Clinical Trial Documentation Authoring
        • Clinical Project Management
        • Independent Data Safety Monitoring Committee
    • Menu iconProduct Authorization / Market Approval
      • Strategy and Consulting
        • Market Access
        • Global Procedure Management
        • Medical Device
      • Pharmacovigilance
        • EU QPPV / National QPPV
        • Literature monitoring
        • Risk Management Support
        • Audit and CAPA Management
        • Medical devices Vigilance
      • Regulatory Affairs
        • CMC Services
        • Health Authority / Agency Interaction
        • Marketing Authorization and Labeling Activities
        • Scientific, Regulatory and Technical Writing
        • Environmental Risk Assessment
        • Leaflet readability testing
      • Quality
        • Commercialization Readiness
        • GxP Services
        • Interim / Contract QA
        • QP Services
      • Medical devices
        • Clinical Evaluation
        • Clinical and Safety Evaluation
        • ISO 13285 QMS
        • Notified Body Interactions
        • Authorized EU Representative
    • Menu iconPost-approval / Maintenance
      • Strategy and Consulting
        • Market Access
        • Medical Device
      • Regulatory Affairs
        • CMC Services
        • Global Procedure Management
        • Health Authority / Agency Interaction
        • Marketing and Labeling Activities
        • Post Approval Commitments and Variations
      • Pharmacovigilance
        • Audit and CAPA Management
        • EU QPPV / National QPPV
        • ICSR Management
        • Literature Screening
        • Pharmacovigilance Set-up
        • Safety Writing
        • Signal Management
        • Medical devices Vigilance
      • Quality
        • GxP Services/Audits
        • Interim / Contract QA
        • QMS Set-up
        • Vendor Management and Oversight
        • Medical device compliance
      • Medical Affairs
        • Medical Information
        • Promotional Material Review
  • Customized
    • Product Expertise
      • Cosmeceutical
      • Small Molecules
      • Biologics
      • Cell, Gene and Tissue Therapies
      • Biosimilar/Follow-on Biologics
      • Medical Devices
      • Drug-Device Combinations
      • In Vitro Diagnostics
      • Companion Diagnostics
      • Foods and Nutraceuticals
      • Vaccines
    • Therapeutic Areas
      • Oncology
      • CNS
      • Infectious Diseases
      • Hematology
      • Autoimmune System
      • Cardiovascular Disease
      • Gastrointestinal
      • Metabolic Disorder
      • Ophthalmology
      • Dermatology
    • Industry Expertise
      • Biopharmaceuticals
      • BioTech Products
      • Biosimilars
      • Consumer Healthcare
      • Genetics
      • Herbal Medicines
      • Vaccines
      • Gene Therapy
      • Small Molecules
      • Medical Device
      • Health Supplements
    • Service Expertise
      • Clinical Trial Support
      • Regulatory Affairs
      • Pharmacovigilance
      • Medical Writing
      • EU Batch Release & Testing
      • Parallel Import
      • Distribution & Supply Chain Support
      • Quality Assurance
      • Early Access/Compassionate Use
      • Orphan Drug Development
  • Contact

Category Archives: Events

You are here:
  1. Home
  2. Category "Events"
Jan302017

Proin ligula iaculis quis ornare id purus

Business, EventsLeave a comment

Nam id sem quis mauris porttitor conse quat id vitae dolor. Phasellus ligula velit molestie rhoncus ullamcorper mauris ultricies mi at pharetra.

Read more
Jan302016

Curabitur laoreet fringilla lorem ipsum

EventsLeave a comment

Porttitor conse quat id vitae dolor. Phasellus ligula velit molestie rhoncus ullamcorper mauris ultricies mi at pharetra.

Read more
Jan72016

Suspendisse turpis ex ultricies nec

Events, International, TechnologyLeave a comment

Aliquam suscipit semper purus, ut tempor ligula condimentum et. Curabitur nulla diam, blandit et sem nec.

Read more
Mar252015

Vestibulum – eget erat non turpis aliquet

EventsLeave a comment

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Maecenas vitae sem dolor. Vestibulum molestie pretium sem in faucibus.

Read more

Our specialists use technology-enabled solutions to guide you through the entire product lifecycle. We deliver extraordinary results — going outside the standard to deliver tailor-made solutions worldwide.

Book a consultation!
Contact Info
  • NL Address:
    Aristotelesstraat 16, 1064 LD, Amsterdam
  • RO Address:
    Bulevardul Unirii 11, Bloc 2B, Sector 4, Bucharest
  • Business hours:
    In line with your global needs!
  • Phone number:
    Tele-Fax : +31 (0) 207729539
    Mobile: +31 (0) 629075858
  • Adverse event reporting
    safety@regpakbiopharma.com
  • General queries
    info@regpakbiopharma.com

Find us on:

Linkedin page opens in new window
Services
  • Discovery / Non-clinical
  • Clinical Development
  • Product Authorization / Market Approval
  • Post-approval / Maintenance
  • Customized Solutions
© RegPakBioPharma. All rights reserved.
  • About
    • NewsWe are lorem isum – lorem amet ipsum dolor porta ullam rutrum glavrida unicus amet from.
    • CareersWe are lorem isum – lorem amet ipsum dolor porta ullam rutrum glavrida unicus amet from.
  • Resources
    • Resources
      • Case StudyGlavrida ipsum nulla – dolor lorem amet ipsum dolor porta ullam rutrum glavrida unicus.
      • Knowledge CenterGlavrida ipsum nulla – dolor lorem amet ipsum dolor porta ullam rutrum glavrida unicus.
  • Our Services
    • All Services
    • Discovery / Non-clinical
      • Strategy and Consulting
        • Non-clinical Development Concept
        • Study Design
        • Scientific Due Diligence
    • Clinical Development
      • Strategy and Consulting
        • Clinical Program Development
        • Statistical Services
        • Medical Device
      • Regulatory Affairs
        • Clinical Trial Applications (CTA)
        • CE Marking
        • Orphan Drug Designation
        • Pediatric Investigation Plan (PIP)
        • Scientific Advice
        • Early Access/Compassionate Use
      • Pharmacovigilance
        • Clinical Trial Safety Support
        • Pharmacovigilance Consulting
        • Medical Devices Vigilance
      • Quality
        • GxP Services
        • Interim / Contract QA
        • Quality Systems
        • Vendor Management and Oversight
        • ISO Compliance for medical devices
      • Clinical Trial Service
        • Site Selection & Clinical Trial Monitoring
        • Clinical Trial Documentation Authoring
        • Clinical Project Management
        • Independent Data Safety Monitoring Committee
    • Product Authorization / Market Approval
      • Strategy and Consulting
        • Market Access
        • Global Procedure Management
        • Medical Device
      • Pharmacovigilance
        • EU QPPV / National QPPV
        • Literature monitoring
        • Risk Management Support
        • Audit and CAPA Management
        • Medical devices Vigilance
      • Regulatory Affairs
        • CMC Services
        • Health Authority / Agency Interaction
        • Marketing Authorization and Labeling Activities
        • Scientific, Regulatory and Technical Writing
        • Environmental Risk Assessment
        • Leaflet readability testing
      • Quality
        • Commercialization Readiness
        • GxP Services
        • Interim / Contract QA
        • QP Services
      • Medical devices
        • Clinical Evaluation
        • Clinical and Safety Evaluation
        • ISO 13285 QMS
        • Notified Body Interactions
        • Authorized EU Representative
    • Post-approval / Maintenance
      • Strategy and Consulting
        • Market Access
        • Medical Device
      • Regulatory Affairs
        • CMC Services
        • Global Procedure Management
        • Health Authority / Agency Interaction
        • Marketing and Labeling Activities
        • Post Approval Commitments and Variations
      • Pharmacovigilance
        • Audit and CAPA Management
        • EU QPPV / National QPPV
        • ICSR Management
        • Literature Screening
        • Pharmacovigilance Set-up
        • Safety Writing
        • Signal Management
        • Medical devices Vigilance
      • Quality
        • GxP Services/Audits
        • Interim / Contract QA
        • QMS Set-up
        • Vendor Management and Oversight
        • Medical device compliance
      • Medical Affairs
        • Medical Information
        • Promotional Material Review
  • Customized
    • Product Expertise
      • Cosmeceutical
      • Small Molecules
      • Biologics
      • Cell, Gene and Tissue Therapies
      • Biosimilar/Follow-on Biologics
      • Medical Devices
      • Drug-Device Combinations
      • In Vitro Diagnostics
      • Companion Diagnostics
      • Foods and Nutraceuticals
      • Vaccines
    • Therapeutic Areas
      • Oncology
      • CNS
      • Infectious Diseases
      • Hematology
      • Autoimmune System
      • Cardiovascular Disease
      • Gastrointestinal
      • Metabolic Disorder
      • Ophthalmology
      • Dermatology
    • Industry Expertise
      • Biopharmaceuticals
      • BioTech Products
      • Biosimilars
      • Consumer Healthcare
      • Genetics
      • Herbal Medicines
      • Vaccines
      • Gene Therapy
      • Small Molecules
      • Medical Device
      • Health Supplements
    • Service Expertise
      • Clinical Trial Support
      • Regulatory Affairs
      • Pharmacovigilance
      • Medical Writing
      • EU Batch Release & Testing
      • Parallel Import
      • Distribution & Supply Chain Support
      • Quality Assurance
      • Early Access/Compassionate Use
      • Orphan Drug Development
    • Featured Expertise
  • Contact
  • Terms & Notices
    • Privacy Policy
Bottom Bar
Go to Top
We use cookies on our website to give you the most relevant experience by remembering your preferences and repeat visits. By clicking “Accept”, you consent to the use of ALL the cookies.
Cookie settingsACCEPT
Manage consent

Privacy Overview

This website uses cookies to improve your experience while you navigate through the website. Out of these, the cookies that are categorized as necessary are stored on your browser as they are essential for the working of basic functionalities of the website. We also use third-party cookies that help us analyze and understand how you use this website. These cookies will be stored in your browser only with your consent. You also have the option to opt-out of these cookies. But opting out of some of these cookies may affect your browsing experience.
Necessary
Always Enabled

Necessary cookies are absolutely essential for the website to function properly. This category only includes cookies that ensures basic functionalities and security features of the website. These cookies do not store any personal information.

Non-necessary

Any cookies that may not be particularly necessary for the website to function and is used specifically to collect user personal data via analytics, ads, other embedded contents are termed as non-necessary cookies. It is mandatory to procure user consent prior to running these cookies on your website.

SAVE & ACCEPT