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Automotive Industry and Food, Safety, and Drug Regulations
Enterprise application providers wanting to address the distinct regulatory requirements of the automotive, food, safety, and life sciences industries need to

drug regulation  controls required for producing drug products, and these regulations are found in the Congressional Federal Register (CFR) 21 in the following parts: Human pharmaceutical products and veterinary products (21 CFR Part 210 and 21 CFR Part 211) Biologically derived products (21 CFR Part 600 and 21 CFR Part 620) Medical devices (21 CFR Part 820) Processed food (21 CFR Part 100) The set of regulations that are currently in effect are called current good manufacturing practices (CGMPs), emphasizing that they Read More...
Regulatory and Compliance
Regulatory compliance covers the requirements for ensuring products and their associated materials comply with both external and internal rules and regulations. It covers regulatory and requirement...
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Documents related to » drug regulation


Recruiting Trends: 4 Methods for Finding the Right Talent
When it comes to finding the right talent, today’s organizations have plenty of options. With the increasing popularity of social networking, however, companies

drug regulation  offerings include background checks, drug testing, US Department of Transportation regulation compliance solutions, driving records, assessments, verifications, credit checks, and international searches. 4. Video (and Virtual) Interviewing Video and virtual interviewing both provide a simple and unique way for recruiters to interview candidates while helping to build the company brand and cut down on recruiting costs. Candidates can be interviewed using video-conferencing (similar to Skype). Or Read More...

High-tech and electronics, chemical, and oil and gas industries each have their fair share of regulatory requirements to meet, and an increasing number include

drug regulation  and Food, Safety, and Drug Regulations . Environment-friendly Chemicals? The issues of environment, health and safet y (EH&S) are what make the chemical industry one of the most liable of all industries. Chemical companies, therefore, have a pressing need for solutions that will streamline and automate compliance processes, as well as enable them to manage their operations more safely, effectively, and in accordance with both national and international regulations and recommendations. The chemical Read More...
Medical Device Manufacturers Can Leverage ERP/CRM Software to Facilitate FDA Compliance
The US Food and Drug Administration (FDA) requires pharmaceuticals and medical device companies to comply with numerous standards. Medical device manufacturers

drug regulation  which the Food and Drug Administration will accept electronic records and electronic signatures as equivalent to paper records and handwritten signatures. The rule governs electronic records throughout their lifecycle from creation through modification, storage, and final transmission to the FDA. The creation of this regulation and the FDA’s encouragement of the use of electronic records and signatures have placed a significant burden on the developers and users of data collection, management, Read More...
Thou Shalt Manage (and Cherish) Thy (Best) Suppliers
In its recent report, Shifting C-level Business Priorities as the Recovery Takes Hold, Saugatuck Technologies claims that top business priorities are returning

drug regulation  new US Food and Drug Administration (FDA) regulation that sternly says “take the drug XYZ off the market… it is not safe!” The manufacturer in this case has to quickly find all relevant contracts, amend them, present them for a review to proper instances, and execute new contracts in its trading network. The mass contract creation ability and the ability to respond to large-scale contract changes in one fell swoop (from contract search results) are essential here to ensure compliance of all Read More...
Financial Reporting-Who Needs It?
Solid financial reporting applications are as different from run-of-the-mill reporting tools as financial accountancy is from bookkeeping. Organizations

drug regulation  management accounting software,financial reporting tools,financial accounting software,sas 70,international financial reporting standards,financial reporting applications,auditing standards,financial reporting regulations,sarbanes-oxley act,financial compliance reporting,statements on auditing standards no 70,property management accounting software,accounting software for property management,accounting practice management software,accounting management software Read More...
The Sarbanes-Oxley Act May Be Just the Tip of a Compliance Iceberg
The Sarbanes-Oxley Act is not the only government regulation that enterprises must comply with. Several others make it imperative that appropriate enterprise

drug regulation  and the food and drug industries are two areas of business where a growing number of government legislations and safety initiatives require organizations to implement industry-oriented ERP systems in order to ensure compliance. The specifics on how these industries address compliance issues will be looked at in the next installment of this series. Part Three of the series Thou Shalt Comply (and More), or Else Read More...
Are You on Track for 21 CFR Part 203 Compliance?
It’s old, it’s new, and it’s the future. Pedigree tracking regulations were originally passed into law through the Prescription Drug Marketing Act of 1987 (PDMA

drug regulation  law through the Prescription Drug Marketing Act of 1987 (PDMA). After two decades of postponing enforcement, the US Food and Drug Administration (FDA) has lifted its final stay. Pharmaceutical companies are expected to be in compliance with 21 CFR Part 203 by the year 2011. Do you have what it takes for compliance? Read More...
Employment Screening Benchmarking Report: 2011 Edition
As background screening and drug testing have become commonplace, many employers have shifted the focus toward making their screening programs and practices

drug regulation  As background screening and drug testing have become commonplace, many employers have shifted the focus toward making their screening programs and practices better—more efficient, more accurate, more flexible, faster and more appealing to both hiring professionals and applicants. The HireRight 2011 Employment Screening Benchmarking Report points to an array of best practices that can help organizations achieve these goals. Read More...
Orchid Orthopedic Solutions Selects CEBOS QMS
Orchid Orthopedic Solutions recently selected CEBOS MQ1 Elements Life Sciences solution to automate its quality management system (QMS) and ensure compliance

drug regulation  for Standardization (ISO), Federal Drug Administration (FDA), good manufacturing practices (GMP), and more. Functionality includes configurable forms and workflows, electronic signatures, audit trails, and validation scripts. The software thus significantly reduces the time required to complete and maintain regulatory compliance while providing staff with visibility to business processes, tasks, and timing.   CEBOS, a division of QAD Inc. , provides a suite of EQMS and environmental, health, and safety Read More...
How to Comply with Data Security Regulations
A remote data backup solution can be compliant with almost any international, federal, or state data protection regulation@and can be compliant with the common

drug regulation  to Comply with Data Security Regulations BizDomainStore.com's Remote Data Backups is the most cost effective, secure, and convenient way to automatically back up your mission critical data Source: BizDomainStore.com Resources Related to How to Comply with Data Security Regulations : Data Security (Wikipedia) How to Comply with Data Security Regulations Data security is also known as : Remote Data , Federal Data , State Data , Most Data , Mirrored Data , Financial Data , Client Data , Enterprise Data , Read More...
ProcessPro ERP Is Now TEC Certified
ProcessPro, an ERP software vendor from Minnesota, United States, recently presented a live demo session of its software ProcessPro ERP to TEC analysts. Here’s

drug regulation  the US Food and Drug Administration (FDA)-regulated environment—food processing with safety lot traceability issues; nutrition and pharmaceutical products, and supplements manufacturers; cosmetic goods manufacturers; and specialty chemicals and products manufacturers. These areas are governed by the US Occupational Safety and Health Administration (OSHA), the Safe Quality Food Institute (SQF), the National Sanitation Foundation (NSF), and the British Retail Consortium (BRC) guidelines. They are also Read More...

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