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1. DoD Directive 5230.9, "Clearance of DoD Information for Public Release", 4/9/1996
- www.dtic.mil
- TITLE: DoD Directive 5230. ...
- SUMMARY: This Directive reissues DoD Directive 5230. 9, April 2, 1982 to update policy and responsibilities for the security and policy review and clearance of official DoD information proposed for official public release by the Department of Defense and its employees under DoD Directive 5122. ...
2. EU Birds Directive – 25 years on - The Royal Society for the Protection of Birds
- www.rspb.org.uk
- Home > Policy > Safeguarding sites > International obligations > EU Birds Directive – 25 years on .
- EU Birds Directive – 25 years on.
- What is the Birds Directive? .
- Where the Directive triumphed .
- Where the Directive failed to stop damaging development .
- Benefits of the Birds Directive .
- Future development of the Birds Directive .
- What the Birds Directive has achieved .
- EU Birds Directive – 25 years on.
- The European Union's 'Birds' Directive is now 25 years old, first coming into force on 2 April 1979.
- The adoption of the Directive, formally known as 'a Directive on the conservation of wild birds 79/405', represented a landmark in European bird conservation.
- Together with its counterpart, the 'Habitats' Directive, the Birds Directive has made a key contribution to conservation in the UK, benefiting wildlife and people. ...
- Twenty-five years on, those who drew up the Birds Directive are to be applauded for producing legislation that is still working for the broader public interest.
- Europa - 25 years of the Birds Directive.
3. STAR TREK - PRIME DIRECTIVE
- www.70disco.com
- PRIME DIRECTIVE.
- Star Fleet personnel may not violate this Prime Directive, even to save their lives and/or their ship unless they are acting to right an earlier violation or an accidental contamination of said culture. This directive takes precedence over any and all other considerations, and carries with it the highest moral.
4. Advance Medical Directive
- www.aging.state.va.us
- Advance Medical Directive.
- The Virginia Advance Medical Directive is your statement about the medical care you want if you have a terminal condition.
- You may download and print the form(legal paper needed) from the following link Virginia's Advance Medical Directive. ... If you click on the “Virginia’s advance medical directive” link and you get an error message telling you that you need Adobe Acrobat Reader, just click on the get acrobat reader button at the bottom to download a copy of the Adobe Acrobat Reader software for free.
5. Amendments to E.Privacy Directive
- www.euro.cauce.org
- Privacy" Directive.
- 4) Within the context of an existing customer relationship, it is reasonable to allow the use of electronic contact details for the offering of similar products or services, but only by the same company or corporation that has obtained the communication details in accordance with Directive 95/46/EC). ...
- Recital 44 (Deletion: LIBE, Am9) Direct marketing activities carried out by political, charity or other organisations, for instance activities aimed at recruiting new members, fund raising or lobbying for votes, are included in the concept of direct marketing as established by Directive 95/46/EC. Messages by political organisations or others for purposes other than direct marketing, for example the expression of views, thoughts and ideas, are not covered by the provisions on unsolicited communications of this Directive.
- These modalities may continue to be useful in certain cases as an additional tool to the general obligations established in this Directive.
- 2) Notwithstanding paragraph 1, where a natural or legal person obtains from its customers their electronic contact details for electronic mail, in the context of the sale of a product or a service, in accordance with Directive 95/46/EC, the same natural or legal person may use these electronic contact details for direct marketing of its own products or services of a similar category, provided that customers clearly and distinctly are given the opportunity to object, free of charge and in an easy manner, such use of electronic contact details when they are collected and on the occasion of each message in case the customer has not initially refused such use.
- Final Text of Directive 2002/58/EC.
- (41) Within the context of an existing customer relationship, it is reasonable to allow the use of electronic contact details for the offering of similar products or services, but only by the same company that has obtained the electronic contact details in accordance with Directive 95/46/EC. ...
- These arrangements may continue to be useful in certain cases as an additional tool to the general obligations established in this Directive. ...
- (45) This Directive is without prejudice to the arrangements which Member States make to protect the legitimate interests of legal persons with regard to unsolicited communications for direct marketing purposes. Where Member States establish an opt-out register for such communications to legal persons, mostly business users, the provisions of Article 7 of Directive 2000/31/EC of the European Parliament and of the Council of 8 June 2000 on certain legal aspects of information society services, in particular electronic commerce,in the internal market (Directive on electronic commerce) are fully applicable. ...
- Notwithstanding paragraph 1, where a natural or legal person obtains from its customers their electronic contact details for electronic mail, in the context of the sale of a product or a service,in accordance with Directive 95/46/EC, the same natural or legal person may use these electronic contact details for direct marketing of its own similar products or services provided that customers clearly and distinctly are given the opportunity to object, free of charge and in an easy manner, to such use of electronic contact details when they are collected and on the occasion of each message in case the customer has not initially refused such use. ...
6. Policies Page - CSRC
- csrc.nist.gov
- Homeland Security Presidential Directive/Hspd-12 .
- (2) To implement the policy set forth in paragraph (1), the Secretary of Commerce shall promulgate in accordance with applicable law a Federal standard for secure and reliable forms of identification (the "Standard") not later than 6 months after the date of this directive in consultation with the Secretary of State, the Secretary of Defense, the Attorney General, the Secretary of Homeland Security, the Director of the Office of Management and Budget (OMB), and the Director of the Office of Science and Technology Policy. ...
- (3) "Secure and reliable forms of identification" for purposes of this directive means identification that (a) is issued based on sound criteria for verifying an individual employee's identity; (b) is strongly resistant to identity fraud, tampering, counterfeiting, and terrorist exploitation; (c) can be rapidly authenticated electronically; and (d) is issued only by providers whose reliability has been established by an official accreditation process. ...
- Departments and agencies shall implement this directive in a manner consistent with ongoing Government-wide activities, policies and guidance issued by OMB, which shall ensure compliance. ...
- (5) Not later than 6 months following promulgation of the Standard, the heads of executive departments and agencies shall identify to the Assistant to the President for Homeland Security and the Director of OMB those Federally controlled facilities, Federally controlled information systems, and other Federal applications that are important for security and for which use of the Standard in circumstances not covered by this directive should be considered. ...
- (6) This directive shall be implemented in a manner consistent with the Constitution and applicable laws, including the Privacy Act (5 U. ...
- (7) Nothing in this directive alters, or impedes the ability to carry out, the authorities of the Federal departments and agencies to perform their responsibilities under law and consistent with applicable legal authorities and presidential guidance. This directive is intended only to improve the internal management of the executive branch of the Federal Government, and it is not intended to, and does not, create any right or benefit enforceable at law or in equity by any party against the United States, its departments, agencies, entities, officers, employees or agents, or any other person. ...
- (8) The Assistant to the President for Homeland Security shall report to me not later than 7 months after the promulgation of the Standard on progress made to implement this directive, and shall thereafter report to me on such progress or any recommended changes from time to time as appropriate. ...
7. Advance Directive Forms
- www.uslivingwillregistry.com
- Advance Directive Forms.
- Preparing an advance directive involves more than simply filling out a form. ...
- While it is usually not necessary to have an attorney help you prepare an advance directive, you may want to consult an attorney if the various forms you obtain do not fit your needs or if you have any special concerns. After you have prepared your advance directive, consider registering it with the U. ... Visit "How to Register" for information on registering your advance directive free of charge. ...
- Here are some sources for advance directive forms:.
- Partnership for Caring is a nonprofit organization that provides state-specific advance directive forms on-line or by mail. ...
- The states listed below are linked to web sites that provide free advance directive forms. ... You should check with an attorney to make sure that the advance directive you prepare complies with the law in your state. Click on your state to download an advance directive form. ...
- Ohio-Advance directive packet with forms.
8. IRIS - Communiqué Manifestation Directive IPR
- www.iris.sgdg.org
- Appel à un rassemblement à Strasbourg contre une Directive très controversée .
- L'association IRIS (Imaginons un réseau Internet solidaire) appelle à manifester lundi 8 mars devant le Parlement européen à Strasbourg pour empêcher l'adoption en l'état de la Directive sur le respect des droits de propriété intellectuelle. ...
- La Directive sur le respect des droits de propriété intellectuelle doit être examinée et votée par le Parlement européen le 9 mars 2004. ... De plus, par la création, au bénéfice des détenteurs de droits de tous pays, d'un « droit à l'information » et d'un droit à l'assignation légale pour obtenir des informations privées sur les citoyens européens, cette Directive viole la protection de la vie privée des citoyens européens. ...
9. Advance Directive Education - California Coalition for Compassionate Care
- www.finalchoices.calhealth.org
- Advance Directive Education.
- Community-Based Coalitions | Advance Directive | Publications and Materials | Public Policy .
- For information on advance health care directive forms, click here.
- The Center for Humane and Ethical Medical Care (CHEC), Santa Monica-UCLA Medical Center, has produced a 15-minute video entitled, Who Will Speak for Robert? The Importance of Having an Advance Health Care Directive. ...
- Advance Directive Materials.
- Advance Directive Policy Development Tool .
- Advance Directive Fact Sheet in Spanish (for consumers) .
- Advance Directive Fact Sheet in Chinese (for consumers) .
- Using the story of Myrtle Anderson, the presentation covers decision-making capacity, the role of surrogate decision-makers, the authority of the health care agent, the advance health care directive, oral directives, and the role of health care providers. ...
- Advance Directive Policy Development Tool.
- Click here for a copy of the Advance Directive Policy Development Tool.
- Assessing decisional capacity is an important aspect of the advance healthcare directive law. ...
- Advance Directive Fact Sheet in Spanish.
- Click here for a copy of the Advance Directive Fact Sheet in Spanish.
- Advance Directive Fact Sheet in Chinese.
- Click here for a copy of the Advance Directive Fact Sheet in Chinese.
10. Statement by EFFI to the Ministry of Trade and Industry on the proposed IPR enforcement directive
- www.effi.org
- The proposed directive: Proposal for a directive of the European Parliament and of the Council on measures and procedures to ensure the enforcement of intellectual property rights (30 January 2003) - in short: IPR enforcement directive .
- To the Ministry of Trade and Industry Statement on the proposed IPR enforcement directive.
- EFFI considers the proposed directive mainly unnecessary since the current legislation on intellectual property rights already requires that sufficiently efficient judicial protections are incorporated into national legislations (e. ... However, because it seems apparent that the directive is really attempted to be made into force we want to comment some parts of it. ...
- We are especially concerned of digital products, which are compared in the directive to e. ...
- Notably the "studies" behind the proposed directive are not about safety or health but about digital products. ...
- The language used in the proposed directive is especially worrying. ...
- This directive does not fulfill these minimum requirements. ... The proposed directive claims without any reference (p. ... We can only wonder the boldness of the drafters of the proposed directive to rely so strongly on the political rhetorics of only one party. ...
- Even though the language of the directive is in some parts quite humorous it is still a serious and far reaching matter. ...
- Finally, we stress that the directive proposal is extremely political in spite of its technical harmonizing goals. ...
- It is hardly a coincidence that the directive proposal comes out just before EU enlargement to Eastern Europe is completed. The requirements set in this directive concern mostly the new member states, which have not been negotiating on the contents of the directive. To compare, the beneficiaries of the proposed directive are mostly multinational companies whose domicile is either within the current EU or North America.
- In the EU parliament the directive is unfortunately on the table of only the committees of industrial and legal affairs. The draft by Janelly Fourtou, chairman of the legal affairs committee, reflects quite to the point where the directive aims at. ... EFFI's stand is exactly the opposite: the directive proposal is first of all too strict and too inaccurate. ...
11. Appendix V - The Software Directive - Technical Specifications
- website.lineone.net
- Appendix V - The Software Directive .
- The purpose for including the Directive in the Appendix is the benefit of the reader. ...
- Council Directive 91/250/EEC of 14 May 1991 on the legal protection of computer programs.
- COUNCIL DIRECTIVE of 14 May 1991 on the legal protection of computer programs (91/250/EEC).
- Whereas, for the purpose of this Directive, the term 'computer program' shall include programs in any form, including those which are incorporated into hardware; whereas this term also includes preparatory design work leading to the development of a computer program provided that the nature of the preparatory work is such that a computer program can result from it at a later stage; .
- Whereas, for the purposes of this Directive, the term 'rental' means the making available for use, for a limited period of time and for profit-making purposes, of a computer program or a copy thereof; whereas this term does not include public lending, which, accordingly, remains outside the scope of this Directive; .
- Whereas the provisions of this Directive are without prejudice to the application of the competition rules under Articles 85 and 86 of the Treaty if a dominant supplier refuses to make information available which is necessary for interoperability as defined in this Directive; .
- Whereas the provisions of this Directive should be without prejudice to specific requirements of Community law already enacted in respect of the publication of interfaces in the telecommunications sector or Council Decisions relating to standardization in the field of information technology and telecommunication; .
- Whereas this Directive does not affect derogations provided for under national legislation in accordance with the Berne Convention on points not covered by this Directive, .
- HAS ADOPTED THIS DIRECTIVE: .
- The provisions of this Directive shall be without prejudice to any other legal provisions such as those concerning patent rights, trade-marks, unfair competition, trade secrets, protection of semi-conductor products or the law of contract. ...
- The provisions of this Directive shall apply also to programs created before 1 January 1993 without prejudice to any acts concluded and rights acquired before that date. ...
- Member States shall bring into force the laws, regulations and administrative provisions necessary to comply with this Directive before 1 January 1993.
- When Member States adopt these measures, the latter shall contain a reference to this Directive or shall be accompanied by such reference on the occasion of their official publication. ...
- Member States shall communicate to the Commission the provisions of national law which they adopt in the field governed by this Directive. ...
- This Directive is addressed to the Member States. ...
12. Clinical Trials Directive: frequently asked questions
- medicines.mhra.gov.uk
- Clinical Trials Directive: Frequently asked questions .
- The MHRA Clinical Trials Unit would like to help prepare for the implementation of the Clinical Trials Directive on 1 May 2004. ...
- What is the purpose of the new Clinical Trials Directive? .
- What steps are being taken to address the concerns of the publicly funded clinical trials community who fear that the transposition of this Directive could unnecessarily delay or stop trials? .
- Will medicines used in trials be monitored under the Directive? .
- What is the purpose of the new Clinical Trials Directive? .
- The main aim of the Directive is to simplify and harmonise the administrative provisions governing clinical trials by establishing a clear, transparent procedure and creating conditions conducive to the effective co-ordination of such clinical trials in the European Community by the authorities concerned. ... Overall, the Directive aims to provide an environment for conducting clinical research that protects participants without hampering the discovery of new essential medicines. ...
- Currently, clinical trials are not directly regulated under the European Community code relating to medicinal products for human use (Directive 2001/83/EC) but are subject to UK national legislation. ...
- The Directive and the proposed implementing Regulations would cover only investigations/studies which are undertaken to ascertain the efficacy or safety of a medicine in human subjects. ...
- If the infusion is for the purpose of modifying the rate of flow for a therapeutic indication such as claudication, it would be deemed a trial under the Directive as the purpose of the study is to establish the efficacy of a particular medicine. ...
- What steps are being taken to address the concerns of the publicly funded clinical trials community who fear that the transposition of this Directive could unnecessarily delay or stop trials?.
- They are looking at options for transposing the definition of sponsor in the Directive; this must be consistent with the Directive. ...
- The EU Directive does require a sponsor to take responsibility for the initiation, management and/or financing of a trial. ...
- The Council and European Parliament intended the Directive to apply to non-commercial research; the recitals to the Directive specifically mention non-commercial clinical trials conducted by researchers without the participation of the pharmaceutical industry. Moreover those drafting the Directive and Commission guidelines constantly considered the impact on non-commercial research. ...
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