PRWeb.com Press Release Feed - PRWeb Press Release Account Feed

DIA Convenes Industry, Academia, and International Regulatory Leaders to Address The Challenges of Future Use Sampling in Clinical Trials

Wed, 31 Aug 2011 13:00:00 GMT

Industry, Academia, and International Regulatory Leaders Address the Challenges of Future Use Sampling in Clinical Trials

(PRWeb August 31, 2011)

Read the full story at http://www.prweb.com/releases/2011/8/prweb8757535.htm

DIA Conference Explores Ways To Ensure Compliance, Efficiency, and Consistency in Clinical Trials Disclosure

Tue, 23 Aug 2011 16:45:00 GMT

Stay Informed of the Latest Requirements and Developments in the Global Clinical Trial Disclosure Environment.

(PRWeb August 23, 2011)

Read the full story at http://www.prweb.com/releases/DIA/Conference/prweb8739941.htm

DIA Brings Best Practices for Clinical Research and Pharmacovigilance to Latin America

Thu, 18 Aug 2011 17:50:00 GMT

DIA is leveraging its initial success in emerging regions such Latin America, where we already offer annual clinical and regulatory congresses.

(PRWeb August 18, 2011)

Read the full story at http://www.prweb.com/releases/DIA/Clinical-Research/prweb8729766.htm

DIA Explores Ways to Facilitate Drug Development and Optimize Dosing in Renal Impairment

Tue, 16 Aug 2011 13:00:00 GMT

Patients with renal impairment are at increased risk for developing drug-related adverse events, says In these patients drug dosage needs to be closely monitored and adjusted to reflect altered pharmacokinetics (PK) and pharmacodynamics (PD) parameters.

(PRWeb August 16, 2011)

Read the full story at http://www.prweb.com/releases/DIA/renalimpairment/prweb8720881.htm

New DIA Publication Provides Benchmark for Computerized Systems in Clinical Research

Thu, 11 Aug 2011 16:45:00 GMT

This latest addition to the DIA library provides a benchmark for requirements of computerized systems used in clinical research.

(PRWeb August 11, 2011)

Read the full story at http://www.prweb.com/releases/DIA/8/prweb8713159.htm

DIA, FDA and EMA Discuss the ICH Guideline for Clinical Safety Data Management

Tue, 19 Apr 2011 17:00:00 GMT

Two-day workshop will explore how a single, common standard for the ICSR could be advanced.

(PRWeb April 19, 2011)

Read the full story at http://www.prweb.com/releases/DIA/4/prweb8322505.htm

DIA And FDA Host Conference on Cargo and Warehouse Theft of Medical Products

Thu, 14 Apr 2011 19:00:00 GMT

Discuss current best practices to ensure progress in reducing the number of cargo thefts by enhancing storage and in-transit security practices and providing a prompt and effective response when a cargo theft occurs.

(PRWeb April 14, 2011)

Read the full story at http://www.prweb.com/releases/2011/4/prweb8307568.htm

DIA Hosts Dried Blood Spot Sampling In The Pharmaceutical Industry: Three Years of Experience and Implementation

Tue, 12 Apr 2011 18:30:00 GMT

This workshop will focus on the three areas primarily impacted by DBS implementation: bioanalytical, preclinical studies and safety assessment, and clinical studies and clinical pharmacokinetics.

(PRWeb April 12, 2011)

Read the full story at http://www.prweb.com/releases/DIA/Pharmaceutical-Industry/prweb8297404.htm

DIA And FDLI Collaborate On First Comprehensive Conference On Biosimilars Since The Enactment Of BPCIA

Thu, 17 Mar 2011 14:00:00 GMT

FDA, industry, lawyers, academics, clinicians, payers, and patients will discuss the challenges and opportunities associated with the introduction of biosimilars to the US.

(PRWeb March 17, 2011)

Read the full story at http://www.prweb.com/releases/2011/03/prweb8215014.htm

Pharmaceutical Industry, Global Regulatory Authorities, and Allied Working Groups Collaborate to Advance Drug Development in Latin America

Wed, 16 Mar 2011 14:00:00 GMT

Key stakeholders will come together to influence the advancement for harmonization initiatives within the Latin American region.

(PRWeb March 16, 2011)

Read the full story at http://www.prweb.com/releases/2011/3/prweb8210180.htm

DIA Asian Regulatory Conference Facilitates Greater Harmonization Of Regulatory Requirements In Asia Pacific Region

Mon, 14 Mar 2011 15:05:00 GMT

Three-day conference is designed to strengthen cooperation between Asian regulatory authorities and the pharmaceutical industry, facilitate discussion on common issues in the regulatory and technical areas in the Asia Pacific region, and encourage greater harmonization of regulatory requirements in the Asia Pacific region.

(PRWeb March 14, 2011)

Read the full story at http://www.prweb.com/releases/DIA/3/prweb8203268.htm

DIA/FDA Statistics Forum 2011 Advances Regulatory Science

Wed, 09 Mar 2011 15:20:00 GMT

This year’s workshop will continue the dialogue on FDA guidance development and regulatory science initiatives, with particular emphasis on the statistical challenges associated with innovative approaches to the design and analysis of clinical trials data.

(PRWeb March 09, 2011)

Read the full story at http://www.prweb.com/releases/dia-fda/statistics2011/prweb8190142.htm

DIA/FDA Co-sponsored Conference Discusses Use of (Q)SAR to Assess Impurities for Potential Genotoxicity

Thu, 03 Mar 2011 14:00:00 GMT

Find out what constitutes an acceptable in silico evaluation and how to incorporate public and proprietary sources of data into an integrated assessment.

(PRWeb March 03, 2011)

Read the full story at http://www.prweb.com/releases/DIA/QSAR/prweb8176367.htm

DIA Names Quintiles’ J. Rick Turner as New Editor-in-Chief of the Drug Information Journal

Tue, 01 Feb 2011 14:00:00 GMT

Dr. Turner intends to broaden the scope of the Drug Information Journal by publishing articles related to some new and hot topics including medical devices and medical device/drug combination products, companion diagnostics, and integrated pharmaceutical medicine, all with a focus on regulatory science.

(PRWeb February 01, 2011)

Read the full story at http://www.prweb.com/releases/drug-information/journal/prweb8103329.htm

DIA Marketing Pharmaceuticals 2011 Explores How Marketing Is Conducted In A Highly Regulated Environment

Wed, 26 Jan 2011 15:00:00 GMT

This three-day conference will explore what is permissible and what is not from a US regulatory and legal standpoint.

(PRWeb January 26, 2011)

Read the full story at http://www.prweb.com/releases/pharmaceutical/marketing/prweb8091182.htm

DIA Launches New Online Professional Networking Platform

Wed, 12 Jan 2011 17:00:00 GMT

DIA ConneX is an interactive global network exclusively populated by DIA members who share professional interests.

(PRWeb January 12, 2011)

Read the full story at http://www.prweb.com/releases/2011/1/prweb8061445.htm

DIA Electronic Document Management 2011 Explores Global Standards Development and Implementation

Tue, 11 Jan 2011 18:00:00 GMT

EDM 2011 is the premier forum for discussing, refining, and advancing emerging standards and processes for the creation, submission, and retention of regulatory information.

(PRWeb January 11, 2011)

Read the full story at http://www.prweb.com/releases/DIA/Document-Management/prweb8058378.htm

DIA and AAPS Co-Sponsored Workshop Explores Solutions to CMC Challenges

Tue, 04 Jan 2011 18:10:00 GMT

Explore all of the challenging topics facing the pharmaceutical and biopharmaceutical communities from development, implementation, and regulatory perspectives.

(PRWeb January 04, 2011)

Read the full story at http://www.prweb.com/releases/cmc-workshop/pharmaceuticals/prweb8044541.htm

DIA Launches New Regulatory Affairs Certificate Program

Tue, 28 Dec 2010 21:00:00 GMT

Comprehensive training on current regulations and their practical application to the development and commercialization of pharmaceutical, biotechnology, medical device, and related health care products.

(PRWeb December 28, 2010)

Read the full story at http://www.prweb.com/releases/DIA/regulatory_program/prweb8038135.htm

DIA Pharmacovigilance and Risk Management Strategies 2011 Will Provide Expert Strategies for Developing and Evaluating Safe Use of Marketed Medical Products

Tue, 14 Dec 2010 18:00:00 GMT

This comprehensive three-day program will discuss the current complexities and controversies in pharmacovigilance and risk management throughout all phases of development and marketed use.

(PRWeb December 14, 2010)

Read the full story at http://www.prweb.com/releases/pharmacovigilance/risk-management/prweb4895434.htm

First International Prescription Drug Labeling Conference Features FDA, HEALTH CANADA, BfArM, AND PMDA

Tue, 26 Oct 2010 16:00:00 GMT

Explore the most pressing issues facing professionals from biopharmaceutical companies, CROs, consulting agencies, and regulatory authorities involved in labeling, clinical safety, regulatory affairs, clinical research and development, and quality control.

(PRWeb October 26, 2010)

Read the full story at http://www.prweb.com/releases/2010/10/prweb4701514.htm

First FDA Co-Sponsored Conference Provides Solutions to Challenges in Patient Recruitment And Retention

Wed, 22 Sep 2010 15:00:00 GMT

Conference on patient recruitment and retention in clinical trials to be held October 14-15, in Rockville, MD.

(PRWeb September 22, 2010)

Read the full story at http://www.prweb.com/releases/2010/09/prweb4548724.htm

DIA Conferences Explore the Life Cycle of Maternal and Pediatric Drug Safety October 12-14 in Bethesda, MD

Fri, 17 Sep 2010 07:01:00 GMT

The Drug Information Association will host two co-located conferences that will provide solutions to the challenges involved in constructing and conducting global pediatric and maternal drug safety programs.

(PRWeb September 17, 2010)

Read the full story at http://www.prweb.com/releases/dia-conference/maternal-drug-safety/prweb4529274.htm

Senior FDA Speakers Discuss Emerging Issues In Cardiovascular Safety And Diabetic Drug Development

Fri, 20 Aug 2010 07:01:00 GMT

The Drug Information Association (DIA), in collaboration with FDA and the Cardiac Research Safety Consortium, will host Development of Type 2 Diabetes Mellitus Drugs Conference: State-of-the-Art Cardiovascular Safety Assessments from October 5-6, 2010 in Washington, D.C.

(PRWeb August 20, 2010)

Read the full story at http://www.prweb.com/releases/DIA/Diabetes/prweb4408284.htm

DIA's Global Approach to Risk Management of Medicines Conference Brings Together Global Regulators and Industry Experts

Tue, 10 Aug 2010 07:00:00 GMT

Learn how to identify and organize essential RMP components as they apply to medicinal products, therapeutic biologics, and vaccines.

(PRWeb August 10, 2010)

Read the full story at http://www.prweb.com/releases/2010/08/prweb4366744.htm

Drug Information Association (DIA) Announces New Clinical Safety and Pharmacovigilance Certificate Program

Sat, 12 Dec 2009 08:00:00 GMT

The Drug Information Association (DIA) today announced the creation of its Clinical Safety and Pharmacovigilance Certificate Program.

(PRWeb December 12, 2009)

Read the full story at http://www.prweb.com/releases/2009/12/prweb3331324.htm

New DIA Vision And Mission Coincides With Start of Paul Pomerantz Tenure As Worldwide Executive Director

Mon, 07 Dec 2009 08:01:00 GMT

Following a two-month transition, Paul Pomerantz, MBA, CAE, officially has begun his work as the new worldwide executive director of the Drug Information Association (DIA).

(PRWeb December 07, 2009)

Read the full story at http://www.prweb.com/releases/2009/12/prweb3299424.htm

DIA Safety Conference To Explore Solutions To Challenges Facing Pharmaocovigilance And Risk Management Strategies

Fri, 20 Nov 2009 08:00:00 GMT

The Drug Information (DIA) will host its 9th Annual Conference on Contemporary Pharmacovigilance and Risk Management Strategies from January 10-13, 2010 in Washington, DC.

(PRWeb November 20, 2009)

Read the full story at http://www.prweb.com/releases/DIA/Safety_Conference/prweb3230364.htm

DIA/PhRMA Workshop to Explore Dried Blood Spot Sampling Implementation and Advances

Sat, 14 Nov 2009 08:00:00 GMT

The Drug Information Association (DIA), in cooperation with PhRMA, will host a workshop on Dried Blood Spot Sampling in the Pharmaceutical Industry: Methodology, Implementation and Best Practices on December 8, 2009 in Washington, DC.

(PRWeb November 14, 2009)

Read the full story at http://www.prweb.com/releases/dia_phrma/dried-blood-sampling/prweb3200984.htm

DIA Conference to Explore Components of Risk Management Plans As They Apply to Medicinal Products, Therapeutic Biologics and Vaccines

Fri, 06 Nov 2009 08:00:00 GMT

Expert speakers from industry, Health Canada, EMEA, FDA, and PMDA will lead presentations at the 2nd DIA Conference on Harmonization of Risk Management Plans to be held December 10-11, 2009 in Washington, DC.

(PRWeb November 06, 2009)

Read the full story at http://www.prweb.com/releases/2009/11/prweb3163264.htm

FDA Commissioner Margaret Hamburg to Deliver Keynote Address at DIA 46th Annual Meeting, June 13-17, 2010 in Washington, DC

Thu, 05 Nov 2009 08:00:00 GMT

Dr. Margaret Hamburg, Commissioner of the US Food and Drug Administration (FDA), will deliver the opening keynote address to more than 8,000 professionals from the biopharmaceutical and related sectors at the Drug Information Association (DIA) 46th Annual Meeting.

(PRWeb November 05, 2009)

Read the full story at http://www.prweb.com/releases/dia-meeting/margaret-hamburg/prweb3156974.htm

DIA 8th Annual Electronic Submissions Conference Addresses Current Developments in eCTD around the World

Sat, 10 Oct 2009 07:00:00 GMT

The Drug Information Association will host the 8th Annual Electronic Submissions Conference from November 17- 19, 2009 in San Diego, CA.

(PRWeb October 10, 2009)

Read the full story at http://www.prweb.com/releases/DIA/Electronic_CTD/prweb3021654.htm

International Experts to Review State-of-the-Art Thinking on Signal Detection and Data Mining

Fri, 02 Oct 2009 07:00:00 GMT

The 2nd DIA Conference on Signal Detection and Data Mining will be held from November 16-18, 2009 in New York, NY. This three-day conference will explore address all aspects of signal detection and data mining, including methodologies, clinical interpretation, and international harmonization initiatives.

(PRWeb October 02, 2009)

Read the full story at http://www.prweb.com/releases/DIA_conference/signal_detection/prweb2978214.htm

Global Regulators to Discuss Benefit-Risk Approaches of Medicinal Products at DIA Workshop

Thu, 01 Oct 2009 07:00:00 GMT

The Drug Information Association (DIA) and the US Food and Drug Administration (USFDA) will host Assessing Benefits and Risks of Medicinal Products in Regulatory Decisions from November 3- 5, 2009 in Bethesda, MD.

(PRWeb October 01, 2009)

Read the full story at http://www.prweb.com/releases/Drug_Information_FDA/Medicinal_Products/prweb2971364.htm

DIA Conference to Provide FDA, EMEA, Health Canada, Emerging Regions, NGO, and Industry Perspectives on Global Vaccine Development

Wed, 30 Sep 2009 18:20:00 GMT

The Drug Information Association (DIA) will present FDA, EMEA, Health Canada, emerging region, NGO, and industry perspectives on Global Vaccine Development at the Global Vaccine Development for World Health Symposium from November 3-4 in Bethesda, MD.

(PRWeb September 30, 2009)

Read the full story at http://www.prweb.com/releases/2009/09/prweb2963384.htm

DIA/FDA/PhRMA Conference To Expand The Role Of Modeling And Simulation In Clinical Drug Development

Wed, 23 Sep 2009 07:00:00 GMT

The Drug Information Association (DIA), in collaboration with FDA and PhRMA, will host Modeling and Simulation in Drug Development: Quantitative Approaches for Decision Making from October 28-29 in Bethesda, MD.

(PRWeb September 23, 2009)

Read the full story at http://www.prweb.com/releases/2009/09/prweb2924974.htm

Key Stakeholders to Discuss Regulatory Issues Related to the Use of Study Endpoints in Multinational Clinical Trials

Thu, 03 Sep 2009 07:00:00 GMT

The Drug Information Association (DIA)] Study Endpoints Special Interest Area Community (SIAC) will host Measuring Study Endpoints in Multinational Clinical Trials: Outcomes Reported from the Viewpoint of the Clinician, Patient, and Caregiver from October 26-27, 2009 in New Orleans, LA.

(PRWeb September 03, 2009)

Read the full story at http://www.prweb.com/releases/2009/09/prweb2822344.htm

DIA Conference to Explore The Science and Scope of Personalized Medicine

Wed, 02 Sep 2009 07:00:00 GMT

The Drug Information Association (DIA) will host Personalized Medicine: Biomarkers and Diagnostics in Drug Development, Regulatory Approval, and Access to Patients from October 15-16, 2009 in Toronto, Ontario, Canada.

(PRWeb September 02, 2009)

Read the full story at http://www.prweb.com/releases/2009/09/prweb2819544.htm

DIA/FDA/PhRMA to Host Progression-Free Survival Oncology Workshop

Thu, 27 Aug 2009 07:00:00 GMT

The Drug Information Association (DIA), in cooperation with FDA and PhRMA, will host Progression-Free Survival Oncology Workshop from October 7-9, 2009 in Bethesda, MD.

(PRWeb August 27, 2009)

Read the full story at http://www.prweb.com/releases/2009/08/prweb2796274.htm

DIA 3rd Annual Clinical Trial Disclosure Workshop Offers Strategies for Creating Effective Registries and Results Databanks

Fri, 21 Aug 2009 07:00:00 GMT

The Drug Information Association (DIA) will host its 3rd Annual Clinical Trial Disclosure Workshop (October 6-8, 2009; National Harbor, MD).

(PRWeb August 21, 2009)

Read the full story at http://www.prweb.com/releases/DIA/clinical_trial_disclosure/prweb2775064.htm