e-Reg: management of Regulatory Affairs' big data

e-Reg: management of Regulatory Affairs' big data
Product Description

OP Pharma has been providing all-around services in the Regulatory Affairs field for more than 20 years to small to big pharma Companies in Italy as well as in the European Union.

Do you have lots of products and/or products' data which you cannot organize/archive internally and of which you would like to outsource the management?
By means of our self-developed IT program e-Reg, we offer customized IT solutions to manage RA big data (including relevant information, dates, documents) of all of your products' practices, renewals, variations, prices, technical information, accountability, pharmacovigilance, API/FP manufacturers, texts etc.. from hundreds of products and thousands of packs.

With the user-friendly interface of e-Reg, you'll have fully-secure, direct online access from the browser to your own data and will easily and quickly find the needed information/document or get an overview of one or all...

O.P. PHARMA S.R.L.

  • Country/Region:
    Italy
  • On CPHI since:
    2021
  • Certificates:
    1
  • Employees:
    1 - 24
Company types
Consultancy
Pharmaceutical company
Primary activities
Contract Research Organisation
Pharmaceutical Company (generic finished products)
Pharmaceutical Company (innovator finished products)
Regulatory Affairs
Specifications

O.P. PHARMA S.R.L.

  • Country/Region:
    Italy
  • On CPHI since:
    2021
  • Certificates:
    1
  • Employees:
    1 - 24
Company types
Consultancy
Pharmaceutical company
Primary activities
Contract Research Organisation
Pharmaceutical Company (generic finished products)
Pharmaceutical Company (innovator finished products)
Regulatory Affairs

More Products from O.P. PHARMA S.R.L. (2)

  • IT/EU REGULATORY AFFAIRS - Support and management of RA practices

    Product IT/EU REGULATORY AFFAIRS - Support and management of RA practices

    OP Pharma has been providing all-around services in the Regulatory Affairs field for more than 20 years to small to big pharma Companies in Italy as well as in the European Union.
    Our expertise ranges from submission of registrations, variations, prices, texts, renewals (also via CESP), to CEP and...
  • IT/EU REGULATORY AFFAIRS - Support and management of Technical documentation and eCTD

    Product IT/EU REGULATORY AFFAIRS - Support and management of Technical documentation and eCTD

    OP Pharma has been providing innovative services in the Regulatory Affairs field for more than 20 years to small to big pharma Companies in Italy as well as in the European Union.
    Our expertise covers the lifecycle management of pharmaceutical products, whole or in part, ranging from digitization ...