Drug Reference definition

Drug Reference means either (i) the generic drug name associated with the INSMED Product, and/or (ii) INSMED’s trademark for such INSMED Product, depending upon the status of INSMED’s branding for the INSMED Product at the time of commercialization by the Parties as contemplated herein. Notwithstanding the foregoing, the Parties shall discuss the precise forms of co-branding to accompany the Device and Nebulizer Handset and the INSMED Products, including support or other promotional materials therefor, to promote the use of the Device and Nebulizer Handset exclusively with the INSMED Product and use of the INSMED Product in the INSMED Field exclusively with the Device and Nebulizer Handset. INSMED shall not modify PARI’s labeling in any way (including by over-labeling). Except as expressly set forth in this Agreement (including, but not limited to Section 3.1), INSMED shall not use any videos, photographs or graphic depictions of the PARI Products without PARI’s prior written approval; provided that such approval shall not be unreasonably withheld or delayed, and PARI’s failure to respond to a request for approval within *** (***) Business Days will be deemed approval.
Drug Reference has the meaning set forth in Section 3.4(a).
Drug Reference means either (i) the generic drug name associated with the Serendex Product, and/or (ii) Serendex’s trademark for such Serendex Product, depending upon the status of Serendex’s branding for the Serendex Product at the time of commercialization by the Parties as contemplated herein. Notwithstanding the foregoing, the Parties shall discuss the precise forms of co-branding to accompany the PARI Products and the Serendex Products, including support or other promotional materials therefor, to promote the use of the PARI Products exclusively for use with the Serendex Product. Serendex shall not modify PARI’s labeling in any way (including by over-labeling), and all support and promotional materials including any of PARI’s trademarks, artwork, images or similar materials must be reviewed and approved by PARI pursuant to agreement by the appropriate subcommittee or otherwise in writing prior to use. Serendex shall not use any photographs or graphic depictions of the PARI Products without PARI’s prior written approval. However, no approval shall be needed for labeling or for use of other materials which were already approved with identical content and format by PARI before.

Examples of Drug Reference in a sentence

  • I understand, however, that the USADA Drug Reference Line is only advisory and that I have the absolute obligation and sole responsibility to avoid the use of any product which may contain a banned substance.

  • I know that if I have any questions about medications and banned substances or practices I may contact the U.S. Anti-doping Agency (“USADA”) Drug Reference Line (▇-▇▇▇-▇▇▇-▇▇▇▇) before, during or after my USOTC and the USOEC ant Northern Michigan University stay.

  • The Nebulizer Handset component of the Device will include the dedicated, unique brand name for the Device and the Drug Reference.

  • Concomitant treatments and prior medications entered into the database will be coded using the WHO Drug Reference List, which employs the Anatomical Therapeutic Chemical (ATC) classification system.

  • I know that if I have any questions about medications and banned substances or practices I may contact the U.S. Anti-doping Agency (“USADA”) Drug Reference Line (719-785-2000) before, during or after my Northern Michigan University stay.

  • As determined by PARI, packaging will include the PARI word-▇▇▇▇ and/or logo and/or the PARI Pharma logo, the EFLOW® Technology trademark, a dedicated, unique brand name for the Device, and the Drug Reference (as defined below).

  • Maintains consistency between Common Drug Reference (CDR) and Master Data Review (MDR) Drug databases e.g. medicine and device descriptions and codes.

  • Always check first with your team doctor or the Drug Reference Line before taking any medication prior to competition.

  • The United States Anti-Doping Agency (USADA) offers a Drug Reference Line (719-785-2000) and a Drug Reference Online (▇▇▇.▇▇▇▇▇▇▇▇▇.▇▇▇) where athletes, coaches, athlete support personnel, parents and medical professionals may check to ensure that proper documentation is on file for their medications and that they are consuming medications that are permitted.

  • Any questions that you may have concerning drug education, banned substances and drug testing procedures can be answered by calling the USADA Drug Reference Line @ ▇-▇▇▇-▇▇▇-▇▇▇▇ or 1-719-785- 2020 (outside the U.S.) or on line at ▇▇▇.▇▇▇▇▇▇▇▇▇▇▇▇.▇▇▇.

Related to Drug Reference

  • Adverse Drug Experience means any of: an “adverse drug experience,” a “life-threatening adverse drug experience,” a “serious adverse drug experience,” or an “unexpected adverse drug experience,” as those terms are defined at either 21 C.F.R. § 312.32 or 21 C.F.R. § 314.80.

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Clinical nurse specialist means a registered nurse with relevant post-basic qualifications and 12 months’ experience working in the clinical area of his/her specified post-basic qualification, or a minimum of four years’ post-basic registration experience, including three years’ experience in the relevant specialist field and who satisfies the local criteria.

  • Clinical evaluation means a systematic and planned process to continuously generate, collect, analyse and assess the clinical data pertaining to a device in order to verify the safety and performance, including clinical benefits, of the device when used as intended by the manufacturer;

  • Clinical categories means the groups into which hospital treatments are categorised by type, e.g., brain and nervous system, kidney and bladder, and digestive system. At the time of writing there were 38 categories in the Medicare clinical categories system.