Capas

InstantGMP™ Celebrates Vita Pros' Enhancement of Electronic Batch Record Software with InstantGMP QMS

Retrieved on: 
Monday, February 26, 2024

CARY, N.C., Feb. 26, 2024 /PRNewswire-PRWeb/ -- InstantGMP™, a leading provider of GMP manufacturing software, is thrilled to announce that Vita Pros, a trusted client with over a decade of experience in private label supplement development and manufacturing, has elevated their Electronic Batch Record (EBR) software by integrating InstantGMP QMS, a cutting-edge Quality Management System (QMS) module.

Key Points: 
  • InstantGMP™, a leading provider of GMP manufacturing software, is thrilled to announce that Vita Pros, a trusted client with over a decade of experience in private label supplement development and manufacturing, has elevated their Electronic Batch Record (EBR) software by integrating InstantGMP QMS, a cutting-edge Quality Management System (QMS) module.
  • CARY, N.C., Feb. 26, 2024 /PRNewswire-PRWeb/ -- InstantGMP™ , a leading provider of GMP manufacturing software, is thrilled to announce that Vita Pros , a trusted client with over a decade of experience in private label supplement development and manufacturing, has elevated their Electronic Batch Record (EBR) software by integrating InstantGMP QMS , a cutting-edge Quality Management System (QMS) module.
  • Jamie Schroetter, Owner of VitaPros, expressed enthusiasm, stating, "Adding InstantGMP QMS to our existing software was a strategic move.
  • Responding to customer demands for guaranteed Good Manufacturing Practices (GMP) compliance, Vita Pros has integrated InstantGMP QMS into their Electronic Batch Record (EBR) software.

ClariMed Announces Liz Wellwood as New Head of Quality and Launches Comprehensive Quality Assurance Services

Retrieved on: 
Monday, January 29, 2024

Liz Wellwood is an accomplished professional with over 15 years of experience in quality management and operations, predominantly in the medical device sector.

Key Points: 
  • Liz Wellwood is an accomplished professional with over 15 years of experience in quality management and operations, predominantly in the medical device sector.
  • Liz will lead ClariMed's quality initiatives and spearhead the development of new Quality service offerings.
  • ClariMed is also introducing a suite of quality assurance services that address each stage of medical device development, meeting stringent quality standards while enhancing usability and user experience.
  • Liz Wellwood commented, "I'm eager to grow ClariMed's Quality practice and continue to align our QA services with human factors in medical device development.

ClariMed Announces Liz Wellwood as New Head of Quality and Launches Comprehensive Quality Assurance Services

Retrieved on: 
Monday, January 29, 2024

Liz Wellwood is an accomplished professional with over 15 years of experience in quality management and operations, predominantly in the medical device sector.

Key Points: 
  • Liz Wellwood is an accomplished professional with over 15 years of experience in quality management and operations, predominantly in the medical device sector.
  • Liz will lead ClariMed's quality initiatives and spearhead the development of new Quality service offerings.
  • ClariMed is also introducing a suite of quality assurance services that address each stage of medical device development, meeting stringent quality standards while enhancing usability and user experience.
  • Liz Wellwood commented, "I'm eager to grow ClariMed's Quality practice and continue to align our QA services with human factors in medical device development.

Greenlight Guru Expands Market Leadership with Strong Momentum in Q3 2023

Retrieved on: 
Tuesday, October 24, 2023

INDIANAPOLIS, Oct. 24, 2023 /PRNewswire-PRWeb/ -- Greenlight Guru, the leading provider of cloud-based quality and clinical software for MedTech companies, announces today strong results in Q3 as the company continues to expand its customer base globally and introduce innovative new AI-powered solutions to the market. The company's growth comes at a time when large medical device companies are moving quickly to modernize legacy systems and improve current processes in order to keep pace with the changing regulatory environment.

Key Points: 
  • INDIANAPOLIS, Oct. 24, 2023 /PRNewswire-PRWeb/ -- Greenlight Guru , the leading provider of cloud-based quality and clinical software for MedTech companies, announces today strong results in Q3 as the company continues to expand its customer base globally and introduce innovative new AI-powered solutions to the market.
  • Greenlight Guru was started in 2013 as a purpose-built QMS solution to provide startup medical device companies with a better way to manage quality and design documentation.
  • Greenlight Guru is also the only software provider in the MedTech industry that is actively leveraging the power of AI across its solutions.
  • "2023 has been a record-breaking year for Greenlight Guru, and that momentum has continued through Q3 as we are acquiring more large global customers at a rapid pace," says David DeRam, CEO of Greenlight Guru.

Trustwell Launches Next Generation of its Gold-Standard Nutrition Analysis & Food Labeling Software, Genesis Foods

Retrieved on: 
Wednesday, April 5, 2023

ALBANY, N.Y., April 5, 2023 /PRNewswire-PRWeb/ -- Trustwell, a leading SaaS provider to the food and supplements industries, has announced the launch of the next-generation platform of its flagship product, Genesis Foods. The new SaaS product introduces a streamlined user interface that offers fast and intuitive product formulation and data entry while assisting users with regulatory compliance by offering built-in data checks and alerts. With this innovative solution, Trustwell continues to revolutionize the food industry by making it easier for businesses to meet regulatory requirements and increase efficiency as they bring new products to market.

Key Points: 
  • Genesis Foods simplifies product formulation and nutrition labeling backed by an unrivaled food and ingredient nutrition database.
  • Genesis Foods automates the process of labeling calculations, ensuring that all nutritional information, ingredients, and allergens are correctly displayed on FDA Nutrition Facts labels.
  • "For businesses that are struggling with the complexity and time-consuming nature of food labeling and recipe management, Genesis Foods is a game-changer."
  • While basic food labeling software can develop simple nutrition labels, Genesis Foods is backed by Trustwell's one-of-a-kind proprietary food and ingredient data set.

Trustwell Expands Professional Service Offerings to Include FSMA 204 Consulting

Retrieved on: 
Thursday, March 30, 2023

SALEM, Ore., March 30, 2023 /PRNewswire-PRWeb/ -- Trustwell, a leading SaaS software provider to the food and supplements industries, has announced expanded professional services to support growing traceability regulatory requirements in the United States. Trustwell's FSMA 204 Professional Services will provide food companies with the necessary support to comply with Section 204 of the Food Safety Modernization Act (FSMA 204), the Food Traceability Rule finalized by the Food and Drug Administration in November 2022. Food companies have until January 2026 to be compliant with the ruling.

Key Points: 
  • Trustwell's FSMA 204 Professional Services will provide food companies with the necessary support to comply with Section 204 of the Food Safety Modernization Act (FSMA 204), the Food Traceability Rule finalized by the Food and Drug Administration in November 2022.
  • These new services will enhance Trustwell's existing offerings that include implementation services, application managed services, labeling services, and a wide variety of online and in-person training offerings.
  • Attendees will also receive a FSMA 204 Toolkit, including a checklist for FSMA 204 planning.
  • Trustwell's FSMA 204 professional services are available now, and interested customers can learn more by visiting https://info.trustwell.com/professional-services/fsma-204-consulting .

Death by CAPA (Corrective and Preventive Action) Seminar - ResearchAndMarkets.com

Retrieved on: 
Thursday, September 15, 2022

The "4-Hour Virtual Seminar - Death by CAPA - Does your CAPA Program need a CAPA?"

Key Points: 
  • The "4-Hour Virtual Seminar - Death by CAPA - Does your CAPA Program need a CAPA?"
  • This 4-hour virtual seminar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company.
  • If your CAPA process needs a CAPA, this seminar is for you.
  • This virtual seminar provides detailed lectures on all elements of a CAPA program and how they connect to other parts of your Quality Management System.

ETQ Delivers Advanced Collaboration in New Release of Industry-Leading Reliance NXG QMS and Launches a New Quality Events Application

Retrieved on: 
Wednesday, June 22, 2022

BURLINGTON, Mass., June 22, 2022 /PRNewswire/ -- ETQ, part of Hexagon, today launched a new release of its award-winning, cloud-native QMS, Reliance NXG, allowing teams to create and edit Google Docs natively in Reliance. The company also launched its newest application, Quality Events, giving quality users the broadest set of deviation management capabilities in the industry.

Key Points: 
  • The company also launched its newest application, Quality Events, giving quality users the broadest set of deviation management capabilities in the industry.
  • The Quality Events application further extends Reliance's market-leading range of functionality to help manage and maintain quality when things unexpectedly go wrong.
  • Quality Events is available for customers on Reliance NXG, Reliance CG, and Reliance 2020.
  • With this release, ETQ has also enhanced Reliance NXG with a more intuitive, user-friendly interface to improve navigation and efficiency.

ETQ Delivers Advanced Collaboration in New Release of Industry-Leading Reliance NXG QMS and Launches a New Quality Events Application

Retrieved on: 
Wednesday, June 22, 2022

BURLINGTON, Mass., June 22, 2022 /PRNewswire/ -- ETQ, part of Hexagon, today launched a new release of its award-winning, cloud-native QMS, Reliance NXG, allowing teams to create and edit Google Docs natively in Reliance. The company also launched its newest application, Quality Events, giving quality users the broadest set of deviation management capabilities in the industry.

Key Points: 
  • The company also launched its newest application, Quality Events, giving quality users the broadest set of deviation management capabilities in the industry.
  • The Quality Events application further extends Reliance's market-leading range of functionality to help manage and maintain quality when things unexpectedly go wrong.
  • Quality Events is available for customers on Reliance NXG, Reliance CG, and Reliance 2020.
  • With this release, ETQ has also enhanced Reliance NXG with a more intuitive, user-friendly interface to improve navigation and efficiency.

FDAnews Announces: 1 Week Until Effective Root Cause Analysis and CAPA Investigations for the Life Sciences, Virtual Workshop June 28-30, 2022

Retrieved on: 
Tuesday, June 21, 2022

FALLS CHURCH, Va., June 21, 2022 /PRNewswire-PRWeb/ -- Effective Root Cause Analysis and CAPA Investigations for the Life Sciences A Virtual Workshop Presented by WCG-FDAnews and ValSource Learning Solutions Tuesday, June 28 – Thursday, June 30, 2022, 11:00 a.m.–4:00 p.m. EDT https://wcg.swoogo.com/root-cause-analytics-capa-investigations-june-2022

Key Points: 
  • Deviations and failures may be a fact of life but understanding what happened, and why, is key to establishing corrective actions and achieving success.
  • Drug and devicemakers will learn how to upgrade their root cause analysis and corrective and preventive action (CAPA) investigations in this virtual workshop.
  • James L. Vesper, PhD, MPH, Director of ValSource Learning Solutions, will lead attendees through a defined, logical process for root cause analysis and CAPA investigations that can be applied in the drug, medical device and clinical trial industries.
  • He will help attendees develop the skills and techniques needed to conduct more effective investigations of quality incidents and identify ways to reduce the likelihood of recurrence.