All About the Quality Management System

Quality Management System refers to a set of processes, policies and procedures that are required for planning and execution in any core business area of a company. It is a system that an organization follows to reduce and eventually eliminate non-conformance to standards, specifications and expectations of a customer in a cost efficient manner. Some […]

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Process Optimization and Automation in Pharmaceutical Manufacturing

Process optimization and automation use computers to control a process by optimizing the specified set of parameters without violating any constraints. These are executed to minimize costs, and maximize output and efficiency. You can automate the supervisory control system to deliver better yields, have more stable plant operations, lower the utility consumption, and ensure that […]

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Utility System Qualification for the Pharmaceutical Industry

Pharma and medical equipment manufacturing is a highly-regulated industry. Given the stress on product quality and the widespread impact of substandard production on public health and safety, utility system qualification is a critical step that companies must take towards ensuring that all their products comply with federal laws and regulations. Utility Systems in Pharma In […]

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Good Manufacturing Practice Compliance Services in Pharmaceuticals

Good manufacturing practice (GMP) is a process for defining the quality standards which must be met by drug manufacturers. GMP standards define the practices which must be undertaken by the drug manufacturers to ensure compliance to the regulatory environment and the fitment of the drug for the intended use. GMP lays down written procedures that […]

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Instrument Qualification for Analytical and Computerized Instruments

The majority of analytical instruments used in laboratories, and many field instruments too, are now digital. The precision and accuracy of measurements are higher, but you need to ensure the instrument you select is suitable for the application. Instrument qualification has become an important part of overall quality, as a gauge for this suitability to […]

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Project Management Services for Maintaining Pharmaceutical Quality

Project management is a set of processes designed to help make a project effectively see the light of day. It is a discipline that widely accepted across various industries and its principles can be applied to any and every sector, especially manufacturing. In addition to assigning responsibility to key stakeholders, it also entails regular monitoring […]

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What is IQ OQ PQ?

For industries involved in pharmaceutical and health care products, or even laboratories, product quality is paramount and minute inconsistencies can have disastrous results. Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ) are an essential part of quality assurance through equipment validation. What Do IQ, OQ and PQ Mean? IQ OQ PQ protocols are […]

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Bay Area Calibration Services Adds To Quality Compliance Services

RS Calibration Services is excited to announce the launch of our new Quality Compliance Consulting Services department, headed by Mr. John Vuong. Vuong, who has over 15 years of experience overseeing the corporate compliance program in a regulatory environment, is a valuable new addition to the Bay Area calibration services company, as he manages a […]

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RS Calibration Services Expanding Quality Compliance Department

RS Calibration Services takes pride in its strict adherence to complying with Food and Drug Administrations (FDA) regulations. The company is dedicated to keeping abreast of the most recent developments governing the requirements for Equipment Validation in the FDA environment. In the ongoing effort to enhance its reputation as a leader in Bay Area Calibration […]

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