Examples of using Common technical document in English and their translations into French
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Colloquial
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Official
Common Technical Document(CTD.
We use it for writing the CTD(Common Technical Document.
Common Technical Document(CTD) M4Q.
Regulatory affairs and common technical document(CTD) structure.
Common Technical Document(CTD) Notice.
Canadian Reference Product(1995-12-04) 9, 13,18 Common Technical Document.
Common Technical Document Summaries.
Transmission of Electronic Data in Electronic Common Technical Document Format.
Common Technical Document(CTD) and eCTD.
Distribute Regulatory Transaction in Electronic Common Technical Document Format.
The Common Technical Document- Quality(CTD-Q.
Health Canada encourages the submission of applications in Common Technical Document(CTD) format.
Common Technical Document Table of Contents.
General Format: Preparation of Product Dossiers in Common Technical Document Format.
The CTD( Common Technical Document) Complexity.
Drug/Medical Device Combination Products(1999-05-01)internal Common Technical Document.
Common Technical Document Summaries?4.3 Module 3.
Preparation of Drug Regulatory Activities in Electronic Common Technical Document.
Electronic Common Technical Document Structure and Leaf Title.
Structure and Content of a Regulatory Activity in Electronic Common Technical Document Format.
O Electronic Common Technical Document Specification(Version 3.0 and 3.2)?
The Common Technical Document- Quality(CTD-Q) Last Updated: 2003-06-10 Important Notices.
Figure 8: Filing Process for Regulatory Transactions in Electronic Common Technical Document(eCTD) Format.
Common Technical Document for the Registration of Pharmaceutical Products for Human Use CTD.
Correct Errors andFile Corrected Regulatory Transactions in Electronic Common Technical Document Format.
Figure 2: Electronic Common Technical Document with One Regulatory Transaction.
All submissions must be provided to Health Canada in an electronic Common Technical Document(eCTD) format.
O Electronic Common Technical Document Specification(Version 3.0 and 3.2) Guidance for Industry M4.
Preparation of Drug Regulatory Activities in Electronic Common Technical Document(eCTD) for a 60-day consultation period.