Examples of Pfizer US in a sentence
Pfizer US will be the sole owner of all Intellectual Property it generates during the development, manufacture, and supply of the Product or otherwise related to the Product.
Moreover, the 2015 tax returns of the Trust show it holds shares and corporate bonds in pharmaceutical companies such as Pfizer (US$ 719,462 base market value), Novartis AG-REG (US$ 6,920,761), Gilead Sciences (US$ 2,920,011 base market value), GlaxoSmith-Kline (US$ 1,589,576 base market value), BASF (US$ 4,909,767), Abbott Laboratories (US$ 507,483), Roche (US$ 7,760,738), Novo Norisdick A/S B (US$ 6,208,992) ,Merck (US$ 782,994).
Address: 6350 Stevens Forest Rd, Suite 301Columbia, MD 21046-2370 Primary Contact Name: Cristina D’Erasmo Phone: 443-259-7872Email:FSF Number:Vendor Name: Novartis Vaccines and Diagnostics, Inc.Address: 350 Massachusetts Ave.Cambridge, MA, 02139-4182 Primary Contact Name: Chris Mikaelian Phone: 877-683-4732Email:FSF Number:Vendor Name: Pfizer U.S. Address: 235 E 42nd StNew York, NY 10017 Primary Contact Name: Paul Hiley Phone: 800-879-3477Email:FSF Number:Vendor Name: Phamatech, Inc.
Reports to Pfizer should be faxed to Pfizer U.S. Clinical Trial Department using the Pfizer-provided Reportable Event Fax Cover Sheet at 866-997-8322.
All serious adverse events (SAEs) and pregnancy reports whether or not considered drug-related should be reported to Pfizer U.S. Clinical Trial Department (contact information below) within 24 hours of receipt by the investigator/sponsor by using the Pfizer SAE form.
All SAEs (expected or unexpected, causally related or not) mustalso be reported to Pfizer’s drug safety vendor, Pfizer U.S. Clinical Trial Department within24 hours of the Investigator’s awareness as follows: Pfizer U.S. Clinical Trial Dept.
Pfizer US shall be entitled to exclusively exploit any such Product IP Rights.
Všetky práva, ktoré spoločnosť Pfizer alebo Pfizer US výslovne neudelila podľa tejto Zmluvy, si vyhradzuje Spoločnosť Pfizer alebo Pfizer US.
Every effort should be made to follow the patient through resolution of the pregnancy (termination or delivery) and report the resolution of the FDA 3500A (MedWatch Form) to Pfizer U.S. Clinical Trial Department as follows: Pfizer U.S. Clinical Trial Dept.
Actually, it is believed that Pfizer (U.S.) established this “Blockbuster Model” first.