Certification, of operatives

The COA or Certificate of Operation allows an air vehicle that does not nominally meet FAA safety standards access to the Nation Airspace System. The COA application process includes measures to mitigate risks, such as sectioning off the airspace to be used by the unmanned aircraft and preventing other aircraft from entering the space. 

DOE Order 5480.20A (DOE 1994b), Selection, qualification, training, and certification of operators. 

Use People must use equipment correctly. They need to be trained. Complex equipment requires detailed training. For example, OSHA requires specific training for forklift operators and training and certification of operators of specific types of cranes. 

The operator must be trained. Many kinds of hoisting equipment require testing and certification of operators. An example is the testing and certifications offered by the National Commission for Certification of Crane Operators. ... 

Match batch size to container size of critical components, using an integral number of whole containers, where possible Double check materials being added to reactor Complete batch loading sheets for each batch run Use of operator sign-off sheets Preweigh reactants before transferring to reactor Verify raw materials (certificate of analysis for critical materials)... 

Currency of operating procedures - annual employer certification of accuracy... 

General criteria for certification bodies operating certification of personnel... 

The certification shall address all ISO/TS 16949 requirements according to Annex 1. Auditors cannot sample requirements of ISO/TS 16949. All requirements have to be checked within the sample of operations chosen during the audit and the sample has to take in sufficient operations and processes that will enable all requirements to be checked. 

The entire quality system shall be assessed at a minimum of once every three years. The audit plan for a supplier has to cover all requirements, all sites, all locations, all operations, all functions, all customers, all processes, all procedures at least once in a three-year cycle, unless it is an upgrade certification (see clause 4.6). Hence the sample of operations taken on each audit has to cover at least Veth of the whole. 

Multi-method certification of 25 elements with information provided on another 22 elements was performed in NIST SRM 2704 (Buffalo River sediment) by NIST laboratories with four co-operating laboratories from USA and Canada (Epstein et al. 1989). 

Validations fall into two types prospective and retrospective. In prospective validation (see flow chart in Figure 2) the validation is done in a sequential manner, involving installation qualification and operational qualification (IQ/OQ) of equipment (e.g., chromatography instrumentation or column hardware). Appropriate calibrations accompany the IQ/OQ. Process qualification, or PQ, involves formal review and approval of a PQ protocol, execution of this protocol, and issuance of a formal PQ report which includes data analysis and recommendations (i.e., approval/certification of the process). If the process is not approved, the report may recommend a redesign or redoing of the validation protocol and, in some cases, a return of the process to process development for further optimization. 

Until U.S. EPA calls in the facility s Part B permit application, where precise permit conditions will be established through a trial burn, owners/operators of interim status BIFs must ensure compliance with emission standards by showing certification of precompliance and certification of compliance. As the deadlines for these certifications have already passed, all interim status BIFs, except for possible extenuating circumstances, should be in the compliance stage. 

Components are received and are quarantined in ABC Pharmaceutical Industries stores until all testing and certificate of analysis requirements are reviewed and have met the acceptance criteria set forth in manufacturing site standard operating procedures. When all acceptance criteria have been met, the components are released by Quality Control and are ready to be issued for production using the procedures specified in manufacturing site standard operating procedures. 

Unlike the IFOAM accreditation program, government-run conformity assessment systems mainly operate at a national level, with no multilateral arrangements in place to facilitate trade of organically certified products recognised by one country into a second country. This has led to a situation in which a certification body operating in one country needs to obtain accreditation after accreditation to enable the products that it certifies to enter into multiple markets as organic. 

---