Compendia definition

Compendia means those resources widely accepted by the medical professions in the efficacious use of drugs which is based on, but not limited to, these sources: the “American Hospital Formulary Services Drug Information,” the “U.S. Pharmacopeia- Drug Information,” the “American Medical Association Drug Evaluation,” and the peer-reviewed medical literature, and information provided from the manufacturers of drug products.

AI-Powered Contracts

Draft, Review & Redline at the Speed of AI

Compendia means those resources widely accepted by the medical profession in the efficacious use of drugs, including the following sources:

Compendia means resources widely accepted by the medical profession in the efficacious use of drugs, including "American Hospital Formulary Services Drug Information," "U.S. Pharmacopeia - Drug Information," "A.M.A. Drug Evaluations," peer-reviewed medical literature, and information provided by manufacturers of drug products.

Examples of Compendia in a sentence

If the product is not included in the specified Compendia, the Bidder upon being awarded the order must provide the reference standards and testing protocols to allow for quality Control.
Compendia of research on academic achievement going back three decades and more argue that the motivation and success of one’s peers has an influence on how a youngster does in school.
Compendia changes must be implemented by the compendia implementation date.
No Trademark Royalty shall be payable on a Licensed Product used in the NOVACEA Territory for development purposes, meaning use of Finished Product by NOVACEA (i) in Phase 1, 2 and 3 Clinical Trials, (ii) in Phase 4 Clinical Trials to be conducted by NOVACEA in the NOVACEA Territory upon Regulatory Authorities’ request and (iii) to obtain Compendia Listings; provided, however, that in all cases, Finished Product is supplied by NOVACEA free of charge to the investigators.
University Housing will not remove any additional furniture from the Resident’s room.
Subject to Sections 2.1(b) and 2.6(c), the JDC shall oversee, coordinate and expedite the Development of, and the making of regulatory filings for, each Product worldwide in order to obtain Regulatory Approvals (or Compendia Listings, as applicable).
The applicable Novartis representative will be included in such notification and will communicate to the Compendia as necessary in order to ▇▇▇▇▇ ▇▇▇▇ the exclusive right to report and update the information for the Licensed Product.
The JDC will also facilitate the flow of information with respect to Development activities being conducted for each Committee-Governed Product and oversee Development activities required to support Regulatory Approvals (or Compendia Listings, as applicable).
NOVACEA shall be solely responsible for determining whether the data package from the Clinical Trials conducted for a given indication supports an Approval for such indication or a Compendia Listing in a given country in the NOVACEA Territory.
NOVACEA shall exercise its good faith judgment consistent with its obligation to use Diligent Efforts in determining whether to cease development of the Licensed Product within an indication set forth in the Development Plan (whether an Approved Indication or Compendia Indication) or to develop new indications that it has decided to develop based on the then available pre-clinical and clinical data.

More Definitions of Compendia

Compendia means those resources widely accepted by the medical profession in the

Compendia means the "American hospital formulary services drug information",

Compendia means those resources widely accepted by the medical

Compendia means resources widely accepted by the medical profession in the efficacious use of drugs, including “American Hospital Formulary Services Drug Information,” “U.S. Pharmacopeia – Drug Information.” “A.M.A. Drug Evaluations,” and peer-re-viewed medical literature.

Compendia means the "American Hospital Formulary Services

Compendia means the "American Hospital Formulary

Related to Compendia

Formulary means a list of covered prescription drugs provided under this plan. The formulary includes generic, preferred brand name, non-preferred brand name, and specialty prescription drugs.
PDMA means the Prescription Drug Marketing Act of 1987, as amended, and the regulations promulgated thereunder from time to time.
Quality Assurance Program means the overall quality program and associated activities including the Department’s Quality Assurance, Design-Builder Quality Control, the Contract’s quality requirements for design and construction to assure compliance with Department Specifications and procedures.
ODMHSAS means the Oklahoma Department of Mental Health and Substance Abuse Services.
HCPCS means the Healthcare Common Procedure Coding System.