Qualer Compliance Technology Can Make a Huge Difference: COVID-19

Qualer Compliance Technology Can Make a Huge Difference: COVID-19

The COVID-19 crisis has jolted all aspects of life. Within the life science and pharmaceutical industries, the repercussions of dealing with the novel coronavirus SARS-CoV2 has taken center stage. The rapidly changing knowledge about the virus and the resulting disease, COVID-19, has meant a race against time to find treatments, vaccines, and supplies to help …

COVID19 Compliance Management Software

Guiding Through the Storm: How the Industry Must Lead in the COVID-19 Crisis

The COVID-19 pandemic has sent shock waves through life as we know it. In turn, the biotechnology industry suddenly faces an unparalleled situation, in which the large focus of industry work bends to address the crisis. On the front lines of research, the race to develop treatments for the disease has sent a ripple effect …

Compliance Management Covid

How Qualer Can Help During COVID-19

How Qualer Can Help During COVID-19 The disruption to life as we know it cannot be understated in the unfolding wake of COVID-19. Your health and safety matter above all other considerations, and we at Qualer wish you and yours good health. Navigating Work in a Crisis In this uncertain time, reliability and assistance are …

GMP Compliance Propels the Life Sciences Market

GMP Compliance Propels the Life Sciences Market

Why is GMP Compliance Necessary? Government regulatory bodies help protect lives by ensuring the safety of pharmaceuticals, medical devices, food, and any other products that could affect health. In order for new products to be put to market, these agencies provide guidelines for regulatory compliance. That is the essential step in ensuring safety.Good Manufacturing Practice …

Audit Readiness Compliance Management

How To Enable Audit Readiness and Full Compliancy

Compliance with regulations is paramount to reliable business, and scientific research in particular. Audits verify that compliance is maintained in facilities. The ideal scenario for an institution is to be as prepared as possible for an audit. This eliminates additional stress, and ensures a smooth audit. Preparing for Audits When preparing for an audit, there …

Compliance Management Validation Documents

Compliant Validation Certificates and Service Event Tracking

Certificates and Service Event Tracking The importance of calibration in scientific disciplines cannot be understated. For scientific accuracy, instruments must function according to their designed use. But calibration goes beyond this, ensuring the essential need for reproducibility of results in scientific research and testing. Scientific assets requiring calibration also need the certification to document their …

Introducing Qualer 2.8 Asset Management Update

In 2020, you can be more efficient and cost effective with Qualer 2.8! This release delivers more robust features, flexibility, and tools to efficiently manage your equipment and calibration processes. You asked and Qualer continues to deliver! Additionally, we have taken security protocols to the next level with new user roles and Qualer’s Identity Service …

Benefits of ISO/IEC 17025 Accreditation

Benefits of ISO/IEC 17025 Accreditation

Accreditation is vitally important for service providers and calibration labs in every industry. Though voluntary, accreditation can often dictate the success of your business and your ability to maintain a steady stream of revenue. Finding new ways to support the growth and quality of your business is one of your most important day-to-day concerns, so …

Why Does a Lab Need Validation Documents & Compliance

Your business requires compliance and validation. But what does validation mean? At its simplest, validation is a method used to regulate electronic records and signatures. So how did this all begin, and what significance does validation hold today? A Brief History of Validation As technology advanced during the early 1990s, it became clear that organization …

FDA Audit Readiness Software

How To Pass Your Next FDA Audit

For asset managers, the FDA and Form 483 can often seem like the boogeyman — just more real and with considerably higher consequences. Enduring and passing FDA audits are a regular part of your job, but they never get easier or less nerve-wracking. Every organization has its own specific compliance needs, but there are a …