Total Results for tag drug: 530

1 2 3 ... 53
  • Channel
    • Select Category first

FILTER

CHANNEL
CATEGORY
2
score
Drug Rounds - Inappropriate Medications in the Elderly
Strategies to reduce inappropriate drug use and reduce ADRS in older adults is the focus of this UPMC presentation by pharmacist, Joseph Hanlon.
06/27/2020
12:00 AM
0
score
Generic Drug Product Development (ANDA) and Paragraph IV Filing Strategy (Exc...
Understand the rationale for Generic Drug Product Development via an ANDA Filing and the potential added value of a Paragraph IV Application, exclusive to the US market.
06/08/2013
12:00 AM
0
score
FDA’s Regulation of Cosmetic Labeling Under the Federal Food, Drug and Cosmet...
Learn FDA labeling requirements for cosmetic products in the United States including general labeling and ingredient-related limitations that federal laws and regulations place on...
06/01/2013
12:00 AM
1
score
Study to Support Shipping and Distributing Pharmaceutical Products
This training on pharmaceutical stability studies will highlight the key factors that would affect the shipping and distribution of drug products. It will explain the stability studies...
05/08/2013
1:00 AM
0
score
Overview of Combination Product Development for Pulmonary Drug Delivery
Learn about market trends for pulmonary drug delivery and development including generic opportunities and commercial development status, the rationale for reimbursement and the groundwork...
04/25/2013
12:00 AM
0
score
What you Need to Know to Successfully Market and Sell an Over-the-Counter Dru...
Learn how to market and sell an Over-the-Counter (OTC) drug product in the United States; and get strategic advice for avoiding FDA enforcement action.
04/20/2013
12:00 AM
0
score
Dietary Supplements Labeling - Avoiding Claims that Invite Scrutiny and Penal...
Learn FDA requirements for labeling dietary supplements. Avoid dietary supplement labeling claims by properly labeling your products for the US market per FDA requirements.
04/13/2013
1:00 AM
1
score
Dietary Supplement Adverse Event Reporting and Recordkeeping Requirements und...
This webinar on dietary supplement adverse event reporting will explain the requirements under federal law as to when serious adverse event reports must be submitted to the FDA, what...
04/05/2013
1:00 AM
0
score
Quality Practices for Research and Development (R&D) CMC Laboratories
chemistry manufacturing and controls, drug development, Chemistry Manufacturing and Controls program, drug development CMC, early trials CMC, CMC process, drug product development, CMC...
03/29/2013
1:00 AM
5
score
Mexico shifts drug war strategy
It was a staggering sight, even in a Mexican city that has seen its share of violence in recent years as drug-related crimes surged.
03/28/2013
9:06 PM
1 2 3 ... 53