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So far Teresa Cain has created 179 blog entries.

Regulatory Education for Industry (REdI): Generic Drug Forum – April 3 & 4, 2019

This event offers practical advice, case studies, and a deep dive into the Abbreviated New Drug Application (ANDA) assessment process. FDA will also discuss science unique to generic drug applications. After this course, attendees will be able to: Discuss requirements for an ANDA Understand and determine when to use a reference listed drug or a [...]

2019-03-14T13:51:11+00:00March 14th, 2019|

Tennessee’s Severe Weather Awareness Week – February 24 to March 2, 2019

Tennessee Gov. Bill Lee announced today that Tennessee's Severe Weather Awareness Week is Feb. 24 to March 2, 2019, and the Tennessee Emergency Management Agency (TEMA), Tennessee Association of Broadcasters (TAB), and the National Weather Service (NWS) are asking Tennesseans to make severe weather planning and preparedness a priority. “Severe weather, natural disasters, and man-made [...]

2019-02-27T21:39:16+00:00February 27th, 2019|

Quality Control Laboratory Compliance – cGMPs and GLPs – March 14-15, 2019 in San Francisco, CA

DA inspection and oversight of quality control (QC) laboratories are essential elements of the agency’s evaluation of the compliance status of regulated companies representing multiple industries - pharmaceuticals, biologics, medical devices, as well as foods and cosmetics - as well as the contract QC laboratories which service these industries. Lack of compliance can result in [...]

2019-02-12T21:00:07+00:00February 12th, 2019|

Call for Abstracts (deadline February 28) – 8th International Conference on Bioengineering and Nanotechnology – May 28-31, 2019 in Baltimore, MD

Presented by the Society for Biological Engineering (SBE), the 8th International Conference on Bioengineering and Nanotechnology will bring together leaders and trainees from cutting edge fields of bioengineering and nanotechnology. Topics to be presented include: biomolecular engineering, translational medicine, cell engineering, immunoengineering, and mechanobiology. The global objective of the conference is to bring to the [...]

2019-01-30T15:49:35+00:00January 30th, 2019|

The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements – February 4-8, 2019 in Arlington, VA

This intensive 4 ½ day course provides quality system professionals with the information needed to develop and maintain a quality system program that conforms with the FDA's Quality System Regulation (21 CFR 820) and International Organization for Standardization 13485:2016, the international standard that spells out the requirements for regulatory purposes for quality management systems. For [...]

2019-01-18T14:29:27+00:00January 18th, 2019|

9th ICBE – International Conference on Biomolecular Engineering – January 6-9, 2019 in Newport Beach, CA

ICBE brings together researchers who are using quantitative approaches to advance the understanding and application of molecular biology. The upcoming conference will be in beautiful Newport Beach, CA. Academic, clinical, and industrial researchers are invited to share their recent discoveries to progress the field in biomolecular science and engineering. For more info:  https://www.aiche.org/sbe/conferences/international-conference-biomolecular-engineering-icbe/2019

2018-12-20T20:34:36+00:00December 20th, 2018|

The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements – December 10-14, 2018 in Arlington, VA

The regulatory world for quality management systems (QMS) is changing fast. To succeed in today's global market, the manufacturers of medical devices must understand those requirements. This intensive 4 ½ day course provides quality system professionals with the information needed to develop and maintain a quality system program that conforms with the FDA's Quality System [...]

2018-12-07T20:46:26+00:00December 7th, 2018|

The Quality System Regulation 21 CFR 820 and ANSI/AAMI/ISO 13485: Navigating Regulatory Requirements – December 3-7, 2018 in Manchester, UK

The regulatory world for quality management systems (QMS) is changing fast. To succeed in today's global market, the manufacturers of medical devices must understand those requirements. This intensive 4 ½ day course provides quality system professionals with the information needed to develop and maintain a quality system program that conforms with the FDA's Quality System [...]

2018-11-28T16:26:40+00:00November 28th, 2018|

Webinar – Final Guidance for Industry: Use of Electronic Health Record Data in Clinical Investigations – December 6, 2018, 1:00 pm to 2:00 pm

The Food and Drug Administration, Center for Drug Evaluation and Research and Small Business and Industry Assistance (CDER SBIA), is pleased to announce this virtual event. Issuing the guidance for industry on the use of electronic health record (EHR) data in clinical investigations is part of the agency's commitment to furthering the advancement and usage [...]

2018-11-28T16:22:01+00:00November 28th, 2018|