Glossary

Sequence

A single set of information and / or electronic documents submitted at one particular time by the applicant as a part of, or the complete application .Any collection of content assembled in accordance with the eCTD specification (ICH and EU) will be described using metadata as defined by the EU envelope.

Source: Harmonised Technical Guidance for eCTD Submissions in the EU

Resources

Take advantage of the knowledge and best practices gained from more than 20 years of research, innovation and development for the health and life sciences sectors.

Glossary

The Life Sciences glossary with terminology, acronyms, for regulatory, quality, compliance, clinical trials, and pharmacovigilance software.

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