Meeting Medical Device Quality Control Regulations
Today, in FDA and ISO regulated environments medical device companies are working hard to meet government and industry standards. In fact, many medical device companies are working too hard. Medical device quality control systems in regulated environments is essential. However, many medical device companies spend inordinate amounts of time creating documents via disjointed applications, searching for prior versions of a document, manually routing documents, manually approving documents, etc. This ad-hoc, "do-it-when-you-get-to-it" processes require far too many man hours and way too much busy work. They also affect quality processes such as Corrective and Preventative Actions (CAPA), change control, audits, and training. On the other hand, MasterControl, a provider of integrated medical device quality assurance software systems and services, provides the tools it takes to streamline medical device quality assurance and regulatory compliance processes in a centralized online system.
MasterControl Makes Medical Device Quality Control Software Systems Easy
The MasterControl's Medical Device quality control system is an integrated quality management suite is a configurable, off-the-shelf, and easy-to-use software solution that facilitates FDA and ISO compliance. It integrates different medical device quality processes and connects different departments involved in the compliance initiative. Our medical device quality assurance software automates, streamlines, and effectively manages document control, change control, training control, audits, corrective/preventive action (CAPA), customer complaints, and other forms-based quality and business processes under a single Web-based platform.
In addition to providing robust software, MasterControl offers cutting-edge validation tools and services that will help ensure FDA compliance. The MasterControl Validation Solution consists of a continuum of products and services that address different levels of validation needs. It gives companies the choice of either automated or manual validation services based on their risk assessments. The medical device quality control solution dramatically cuts the time involved in validating a system, reduces risks of project implementation, and makes it easier to validate software upgrades, all of which help lower validation cost.
About MasterControl's Medical Device Quality Assurance Software Systems
MasterControl Inc. is a global provider of GxP process and document management software solutions helping regulated companies experience validated medical device quality control software as they work to develop, produce, and distribute products that are often the result of millions of dollars and years of careful research. With more than a decade of experience within the stringently regulated FDA environment, MasterControl has the expertise necessary to provide the peace of mind medical quality assurance brings.
MasterControl's complete offering of the medical device quality control software system combines the innovation and quality that organization need in order to provide within industries that literally touch the lives of everyone. MasterControl provides solutions specific to the industry of each company.
MasterControl developed the following solutions to provide the medical quality assurance regulated companies seek:
- Contrôle des documents
- Change Management Control
- Corrective/Preventative Action Control
- Audit Control
- Training Control
- Customer Complaints Control
- Bill-of-Materials (BOM)
- Gestion de projets
Medical Device Quality Control Software Services
In order to provide complete solutions to common concerns about medical device quality assurance, MasterControl also offers implementation, training, technical support, and validation services.
Learn More About Medical Device Quality Assurance Software Systems
To learn more about sustaining medical device quality assurance, contact a MasterControl representative today.