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Regulation in the life sciences industry aims to not only ensure the safety and efficacy of products, but also to ensure innovative therapies can pass through investigative and regulatory processes as quickly as possible.
The ultimate purpose of regulatory agencies is usually to protect the health, safety, and property of the public. In a free market economy, many sectors need no regulatory oversight because they self-regulate. Substandard products or services are forced out of the market when customers take their business elsewhere.
Regulatory compliance requires companies to analyze their unique requirements and any mandates specific to their industry and then develop processes to meet these requirements.
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The Regulatory Services Division (RSD) provides oversight using a three-strategy approach: 1) Issuance 2) Modernization and 3) Compliance and Enforcement. The Regulatory Services Issuance section is responsible for issuing regulatory licenses and permits, and for tracking the number of license and permit holders.
Regulatory compliance refers to following the set of governmental laws, regulations, and standards related to a businesss operations. These rules protect sensitive information and establish safety protocols, making them essential.
Regulatory Services means (i) the education of employees on Regulatory Authority issues, (ii) providing summaries of new and amended regulations and responsibilities, (iii) performance of regulatory audits, (iv) preparing fleet analysis with regard to Regulatory Authority regulations and mandatory requirements, (v)
The Regulatory Services Department protects the health, safety and welfare of residents through a program of regulation, inspection, and enforcement of laws and ordinances tied to housing inspection, fire inspections, traffic control, problem properties, and animal care and control.

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