'Regulatory affairs' diaporamas de présentation

Combating the Drug Shortage Crisis

Combating the Drug Shortage Crisis. Moderator Ron Hartmann, PharmD , Senior Vice President, Pharmacy, MedAssets Panelists Valerie Jensen, RPh , Cpatain , USPHS, Associate Director, Drug Shortages Program, FDA

570 views • 43 slides

Kitchen Nightmares

458 views • 27 slides

CAREERS IN PHARMACY

CAREERS IN PHARMACY. N.SANTHI PRIYA ,Mpharm ASSISTANT PROFESSOR CHALAPATHI INSTITUTE OF PHARMACEUTICAL SCIENCES. PHARMACY. Pharmacy is a versatile,dynamic,growing and increasingly diverse profession It has transformed into Global healthcare hub

451 views • 25 slides

Global Warming

343 views • 22 slides

Taking the pulse of bioscience education in America: A State-by-State Analysis

501 views • 20 slides

Pharmaceutical courses and training institute, Thane

We at Raaj GPRAC (Global Pharma Regulatory Affairs Consultants) in Thane, India offer pharma consulting, regulatory affairs services. We also conduct various workshops and seminars on pharma courses. Our Pharmaceutical Education arm conducts 6 months diploma courses in CTD/eCTD and regulatory affairs, also we conduct fast track pharma courses, distance learning programs for working professional and part time courses pertaining to Pharma and Biotech industry for students and working professionals.

516 views • 20 slides

PERMIT REQUIRED CONFINED SPACE Duties of: Supervisor, Attendant and Authorized Entrant

PERMIT REQUIRED CONFINED SPACE Duties of: Supervisor, Attendant and Authorized Entrant. Presented By: Consultation Education and Training Division Michigan Occupational Safety & Health Administration Michigan Department of Licensing and Regulatory Affairs www.michigan.gov/miosha (517) 322-1809.

185 views • 18 slides

AICP New England 13 th Annual Education Day

AICP New England 13 th Annual Education Day. PRIVACY Jenny Erickson Vice President, Legislative and Regulatory Affairs The Life Insurance Association of Massachusetts. Massachusetts General Laws Chapter 93H . Security Breaches Approved by the Governor, August 2, 2007.

290 views • 18 slides

How can we

How can we . Manage Performance. in Regulatory Affairs?. Katlego Ramorola. Performance management. through innovative solutions . Reality:. Performance Management is never done correctly. Employees and Managers both HATE appraisal time!.

237 views • 16 slides

FDAnews

291 views • 14 slides

Sharyland Utilities, L.P. Transition Timeline

Sharyland Utilities, L.P. Transition Timeline. Bridget Headrick Director, Regulatory Affairs. Customer Outreach and Education. Implementation Items. ESI ID and REP Tasks. Participant Testing. ERCOT Transition Scenarios for Sharyland. Paula Feuerbacher Strategic Projects Senior Advisor.

282 views • 11 slides

Making Your K Award Application More Attractive

Making Your K Award Application More Attractive. C. A. Hornung, PhD, MPH Professor, Dept. of Epidemiology and Public Health and of Medicine. Bench to Bedside to Community and Back. T-1 Bench to Bedside Proof of Concept . T-2 Bedside to Community Proof in Practice. CERTS.

213 views • 8 slides

459 views • 7 slides

Presentation by Smile Communications to Portfolio Committee on Communications Lee-Ann Cassie Head of Regulatory Affairs

Presentation by Smile Communications to Portfolio Committee on Communications Lee-Ann Cassie Head of Regulatory Affairs. Smile Overview Who we are?. To be a low cost telecoms operator that will reduce the cost of communisations to provide affordable communications to BoP consumers. Vision.

286 views • 7 slides

Statement of AABB before the Cellular, Tissue and Gene Therapies Advisory Committee

Statement of AABB before the Cellular, Tissue and Gene Therapies Advisory Committee. Joseph Giglio, MS MT(ASCP), CSQE(ASQ)CQA Deputy Director of Regulatory Affairs, AABB March 30, 2007.

214 views • 7 slides

C-TPAT: Past, Present, & Future

Presented by: Robert A. DeCamp, Director of Regulatory Affairs & Consulting A.N. Deringer, Inc. C-TPAT: Past, Present, & Future. History. Where were you on 9/11/01?.

612 views • 6 slides

Webinar On 10 Steps to an FDA-Acceptable Clinical Trial Prot

The clinical trial protocol is a multi-dimensional document that plays a critical role in the success of a clinical trial. There are many schools of thought about the best approach to writing a clinical trial protocol depending on individuals or organizations sponsoring a given clinical trial.

244 views • 2 slides

Webinar On 10 Steps to an FDA-Acceptable Clinica

The clinical trial protocol is a multi-dimensional document that plays a critical role in the success of a clinical trial. There are many schools of thought about the best approach to writing a clinical trial protocol depending on individuals or organizations sponsoring a given clinical trial.

217 views • 2 slides

Webinar On FDA Approval Process for Combination Products

This 2 hours webinar will provide a comprehensive understanding of the FDA Combination Product system. Participants receive a foundation of knowledge about the FDA Office of Combination Products, the FDA Combination Product system, Combination Product submissions, and the scientific and regulatory principles involved.

213 views • 2 slides

Abbreviations

219 views • 1 slides