CPHI Milan 2
CPHI Milan newsletter
PCI High Potent Manufacturing
LB Bohle – 10.06.2025
Temax_Krautz

Current Edition

Current Edition

Subsection - CDMO

Examining how innovative technologies, integrated manufacturing approaches and AI are shaping manufacturing.

Continue reading

Subsection - Injectables

Exploring advances in injectable drug delivery and sterile manufacturing, designed to improve patient-centric delivery.

Continue reading

Subsection - Neurodegenerative Diseases

Exploring emerging approaches to neurodegenerative disease research and treatment.

Continue reading

Subsection - Nasal & Pulmonary

Highlighting how advances in nasal and pulmonary drug delivery, formulation, devices and analytics are enabling more complex therapies.

Continue reading

Advertisement

CPHI 2027
DDL 2026

Advertisement

Nipro August 26

Advertisement

Merxin March 2026

Advertisement

Aurisco 300×250

Advertisement

Lifecore Biomedical

EXTEDO. Redefining Regulatory Information Management

EXTEDO is the key software and service solutions provider in the field of Regulatory Information Management. The complete EXTEDOsuite covers: Product Registration Planning & Tracking, Submission Management, Pharmacovigilance Management, Labeling Management and Document Management.
Today EXTEDO serves more than 700 customers in 57 countries including EMA and more than 25 Regulatory Authorities worldwide.
EXTEDO is the key software and service solutions provider in the field of Regulatory Information Management. The complete EXTEDOsuite is unique in all that it covers within eRegulatory Affairs:
• Product Registration Planning & Tracking
• Submission Management, (eCTD, CTD, NeeS, CADDY,  ePRISM, eIndex, eNTA, vNeeS)
• Pharmacovigilance Management (SUSAR, ICSR, PSUR, E2B)
• Labeling Management and
• Document Management
The EXTEDOsuite is comprised of modules that can be implemented separately or as one Regulatory Information Management platform. The platform allows companies to easily plan, enter, import, share and track relevant regulatory data requested by standards like XEVMPD or IDMP. We provide configurable Off-the-Shelf products, as well as customized and integrated solutions. EXTEDO also provides EURS is Yours, the validation, review and approval system for the EMA and more than 25 Regulatory Authorities worldwide.
Today we serve more than 700 customers in 57 countries ranging from small companies with less than 25 employees to large multinational organizations.  EXTEDO operates in the following areas of life sciences: pharmaceutical, biotech and biopharma, generics, homeopathics, medical devices, healthcare, and public sector. EXTEDO is recognized as one of the worldwide leaders in each of our areas of operation.
PRODUCTS
Registration Planning & Tracking
DRAmanager is a planning and tracking solution that enables you to manage regulatory tasks associated with medicinal product and medical device development. DRAmanager accurately and efficiently keeps registered products compliant from a submission, labeling, and drug safety perspective.
MPDmanager is a standardized database that allows the guided entry and automated imports of all regulatory data requested by XEVMPD and IDMP. For the management of additional product attributes, it enables you to comply with corporate standards.
Pharmacovigilance & Drug Safety
PcVmanager is a drug safety management solution that enables you to classify, create, review, submit, and maintain pharmacovigilance data and adverse event reports in accordance with E2B and MedDRA standards.
Submission Creation & Lifecycle Management
eCTDmanager enables you to easily build, view, validate and publish compliant submissions based on CTD, eCTD, NeeS, IMPD, CTA, eNTA, VNeeS and other submission structures.
DOCmanager is an add-on for eCTDmanager that allows the creation and maintenance of many child dossiers based on one parent dossier and reduces update times for variations.
PlantOS 3 is an off-the-shelf solution that manages the assembly and compilation of electronic dossiers. The following digital standards for regulatory affairs in Crop Science are supported and can be exported from one single data collection (based on the OECD CADDY table of contents): e-PRISM (USA), e-Index (CAN), CADDY.xml (EU) Submission Reviewing & Validation EURS is Yours serves as a complete eCTD validation and reviewing software solution. It reports whether a submitted eCTD- or NeeS-based application conforms to the offi cial format.
EURSvalidator supports you in validating medicinal and veterinary eSubmissions. The validator is used by the majority of European National Authorities including EMA to ensure eCTD and NEES compliance. GLOBALvalidator is an add-on for EURSvalidator that provides enhanced functionality and additional validation sets.
CONTACT For more information, please check our website www.extedo.com, email us: info@extedo.com or call us:
EXTEDO GmbH (European & Global Headquarters) Einsteinstrasse 30, 85521 Ottobrunn, Germany Phone +49 89 189454-0       EXTEDO Inc. (North America Headquarters) 1235 Westlakes Dr., Suite 285, Berwyn, PA 19312, USA Phone +1 (855) 328 3500

Advertisement

MedPharm 16/07

Advertisement

Biopharma group march 2026

Advertisement

Silgan March 2026

Advertisement

Terumo 06/26

Advertisement

Scott Pharma – 25.03.2025

Advertisement

Bespak

Advertisement

Solstice

Advertisement

Bachem skyscraper
Tjoapack
Aptar – 08/01/2026