Healthcare and Medical


How to get a CLIA Waiver for your Medical Device: One and a Half Day In-person Seminar

FDA has granted precious few applications for waiver since their CLIA Waiver guidance was published on January 30, 2008....

Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices: 2-day In-person Seminar

Federal regulation of the advertising and promotion of pharmaceuticals and medical devices reflects an aggressive attitude on the part...

Medical Device Risk Management A to Z – Best Practices for Effectiveness and Efficiency: 2-day In-person Seminar

FDA views risk management as an essential process both during inspections and in the review of pre-market submissions. Effective...

Article : Avoiding FDA Warning Letters

U.S. Food and Drug Administration (FDA) warning letters can spell big trouble for medical device manufacturers and pharmaceutical companies...

Roadmap of California Medical Leaves – One and a Half Day In-Person Seminar

This comprehensive interactive training workshop will help clarify California specific leaves, how they interact with the Federal medical leaves...

Medical Device Conclave – 2015

The medical device industry continues to experience rapid growth rates. This success has brought along with it a number...

Latin America: Regulatory Compliance Requirements for Life Science Products

This two-day comprehensive Course on Latin America Regulatory compliance requirements will cover topics ranging from pre-clinical and clinical requirements...

Why is FDA at my facility, and what do I do during an inspection?

This two day course will prepare firms for a quick, productive, and efficient FDA inspection. Included are segments on...

How to get a CLIA Waiver for your Medical Device

FDA has granted precious few applications for waiver since their CLIA Waiver guidance was published on January 30, 2008....

Medical Device Risk Management A to Z – Best Practices for Effectiveness and Efficiency

FDA views risk management as an essential process both during inspections and in the review of pre-market submissions. Effective...

Process Validation for Medical Devices

Medical device manufacturers can avoid FDA Warning Letters, 483s and enforcement actions with a good understanding process validation principles....

Article: 5 Steps To Establish A Patient Safety Culture

Patient safety is a key component of quality and encompasses the prevention of harm to patients which can occur...

Article: Strengthen your Food Safety Program with GFSI

Adhering to the GFSI benchmarking in food safety enables companies to perform with discipline, and be more efficient and...

Global Medical Device Regulations: One and a Half-day In-person Seminar

Understanding global medical device regulations and requirement and adequate implementation of applicable medical device regulations can significantly expedite the...

7 Tips to go from “Getting By” to “Thriving”

Optimizing revenue cycle performance has become even more critical for practices. Especially with today’s changing healthcare landscape of ICD-10,...

HIEs: Transforming Clinical Workflows for Care Coordination

Providers like Dignity Health, Inspira Health Network, and PinnacleHealth are leveraging their HIEs to help solve care-coordination problems, helping...

20 Practical Tips on Single Sign-On and Strong Authentication from Healthcare IT Professionals

This whitepaper features Imprivata customers who have successfully deployed Imprivata OneSign® Single Sign-On (SSO) and strong authentication at their...

How Agile Insurers are Improving the Bottom Line

The Internet has empowered consumers with self-service, and the insurance industry is adapting and innovating amongst its competitors to...

The Total Cost of Ownership of EHR in a Meaningful Use World

The central theme of industry wide adoption of EHRs is based on the concept of “meaningful use,” which by...
 
Page 2 of 512345