A No-Deal Brexit and the Impact on Medical DevicesEMMAIntl
High risk medical devices are certified by an independent conformity assessment conducted by notified bodies (NB). The notified bodies are overseen by the national authority of each member state in the EU, and by the Medicines and Healthcare products Regulatory Agency (MHRA) in the UK. NBs are also subjected to European commission audits...
As the UK Government prepares to publish the 'Repeal Bill' to give legal effect to the UK's withdrawal from the European Union, this paper looks at the possible implications for pharmaceuticals regulation. The paper by Andrew Hollingsworth gives a short overview of the current EU regulatory framework and looks at some of the options and potential outcomes in the forthcoming UK-EU negotiations.
Medical literature monitoring and entering negative reaction reportsPEPGRA Healthcare
1. A novel process where European Medical Agency offers a new service.
2. The service is focused around medical literature monitoring.
3. This service is also a vital step to ensure that there is no duplication of negative reaction reports.
4. This service came into effect from 1st September, 2015.
To Continue Reading : https://bit.ly/39C4iVW
Pharmacovigilance Literature Search Services - https://bit.ly/2wM7IIH
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Website : https://bit.ly/33Fwsye
Email us: sales.cro@pepgra.com
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Impact of Brexit, Swixit, Turkxit for the European Medical Device MarketGreenlight Guru
The European Union is in transition now due to some regulatory changes. EU MDR will be applicable by May 26th, 2021, but in the meantime, other political situations may impact this timeline.
Manufacturers that would like to register their product in Europe need to understand the potential situations that could happen and how this can change your regulatory strategy.
Brexit will apply by January 1st, 2021. Swixit and Turkxit will depend on the EU commission, but this may happen by May 26th, 2021.
This presentation takes a deep dive into the implications of Brexit, Swixit, Turkxit for the European Medical Device Market.
This free in-depth webinar, presented by Monir El Azzouzi , Founder of Easy Medical Device, will cover the current (Winter 2020) Brexit, Swixit, and Turkxit situation for the European Medical Device Market.
This presentation originally aired during the 2021 State of Medical Device Virtual Summit.
Speculation has abounded in recent weeks regarding the short and long term consequences of Brexit. For the pharmaceutical industry, there are ramifications both in the UK and across continental Europe.
R. Villano - SYNTHETIC STUDY Pharmaceutical reforms in Italy XIX-XXI centur...Raimondo Villano
93. R. Villano “Reforms of Pharmaceutical Service from Italy Union to 21st century” (synthetic study). Starting from a general survey on the pre-Community situation from the beginning of the nineteenth century, the developments of the pharmaceutical service in the Kingdom of Italy and the Italian Republic until 2008, as well as the main interrelations and influences of the Community from the Treaties of Rome of 1957 onwards, are examined. Thus, from legislative unification comes the establishment of the national health service, the initial steps to contain pharmaceutical spending, deregulation, to online pharmacies and liberalization. For a more thorough and reasoned discussion, it is also necessary to frame the essential terms of the main business and / or ‘collateral’ phenomena underlying the pharmaceutical service. Finally, a detailed and detailed analysis is reserved for the treatment of the last three decades. (1,42 Mb; 1 file, 60 slides), Chiron dpt Ph@rma, Roma, January 2018;
A No-Deal Brexit and the Impact on Medical DevicesEMMAIntl
High risk medical devices are certified by an independent conformity assessment conducted by notified bodies (NB). The notified bodies are overseen by the national authority of each member state in the EU, and by the Medicines and Healthcare products Regulatory Agency (MHRA) in the UK. NBs are also subjected to European commission audits...
As the UK Government prepares to publish the 'Repeal Bill' to give legal effect to the UK's withdrawal from the European Union, this paper looks at the possible implications for pharmaceuticals regulation. The paper by Andrew Hollingsworth gives a short overview of the current EU regulatory framework and looks at some of the options and potential outcomes in the forthcoming UK-EU negotiations.
Medical literature monitoring and entering negative reaction reportsPEPGRA Healthcare
1. A novel process where European Medical Agency offers a new service.
2. The service is focused around medical literature monitoring.
3. This service is also a vital step to ensure that there is no duplication of negative reaction reports.
4. This service came into effect from 1st September, 2015.
To Continue Reading : https://bit.ly/39C4iVW
Pharmacovigilance Literature Search Services - https://bit.ly/2wM7IIH
Contact Us:
Website : https://bit.ly/33Fwsye
Email us: sales.cro@pepgra.com
Whatsapp: +91 9884350006
Impact of Brexit, Swixit, Turkxit for the European Medical Device MarketGreenlight Guru
The European Union is in transition now due to some regulatory changes. EU MDR will be applicable by May 26th, 2021, but in the meantime, other political situations may impact this timeline.
Manufacturers that would like to register their product in Europe need to understand the potential situations that could happen and how this can change your regulatory strategy.
Brexit will apply by January 1st, 2021. Swixit and Turkxit will depend on the EU commission, but this may happen by May 26th, 2021.
This presentation takes a deep dive into the implications of Brexit, Swixit, Turkxit for the European Medical Device Market.
This free in-depth webinar, presented by Monir El Azzouzi , Founder of Easy Medical Device, will cover the current (Winter 2020) Brexit, Swixit, and Turkxit situation for the European Medical Device Market.
This presentation originally aired during the 2021 State of Medical Device Virtual Summit.
Speculation has abounded in recent weeks regarding the short and long term consequences of Brexit. For the pharmaceutical industry, there are ramifications both in the UK and across continental Europe.
R. Villano - SYNTHETIC STUDY Pharmaceutical reforms in Italy XIX-XXI centur...Raimondo Villano
93. R. Villano “Reforms of Pharmaceutical Service from Italy Union to 21st century” (synthetic study). Starting from a general survey on the pre-Community situation from the beginning of the nineteenth century, the developments of the pharmaceutical service in the Kingdom of Italy and the Italian Republic until 2008, as well as the main interrelations and influences of the Community from the Treaties of Rome of 1957 onwards, are examined. Thus, from legislative unification comes the establishment of the national health service, the initial steps to contain pharmaceutical spending, deregulation, to online pharmacies and liberalization. For a more thorough and reasoned discussion, it is also necessary to frame the essential terms of the main business and / or ‘collateral’ phenomena underlying the pharmaceutical service. Finally, a detailed and detailed analysis is reserved for the treatment of the last three decades. (1,42 Mb; 1 file, 60 slides), Chiron dpt Ph@rma, Roma, January 2018;
2010 and 2011 eu competition law and case law developments with a nexus to po...Michal
This third overview of EU competition and sector-specific regulatory jurisprudential
and case law developments with a nexus to Poland covers the years 2010 and 2011.
This period of time is worth noting for several reasons. First, EU courts delivered
a significant number of judgments in ‘Polish’ cases including an increased number of
preliminary rulings. Second, 2010-2011 developments were dominated by judgments
and decisions concerning telecoms. Finally, the Commission adopted only a handful
of Polish State aid decisions following a formal investigation procedure under
Article 108(2) TFEU.
Thomas Schael - Eye for Pharma Berlin 2013: A regional payers’ perspective of...Thomas Schael (PhD)
Thomas Schael's presentation on insights and actionables on drug expenditure and the requirements of Italian payers for market access at the Payers' Forum Europe 2013 in Berlin.Thomas Schael discusses Italy’s drug distribution system and explains how he dramatically cut spending on drugs. Schael gives his outlook on the major challenges for drug expenditure in Italy and Europe and offers advice to the pharmaceutical industry on how to work better with authorities.
Illegible prescription could lead to deficiency in serviceArunSharma10
Illegible prescription could lead to medical negligence and deficiency of service
Misinterpretation by the pharmacist
Wrongful dispensing of medicines by pharmacist
National Consumer Disputes Redressal Commission
Delhi State Consumer Disputes Redressal Commission
Consumer court
Medical negligence
Medical negligence in nephrology
Bad handwriting in prescription
Opportunities for Reform and Optimization presented by Mohammed El Said from the University of Central Lancashire (UCLAN) UK. Presentation includes:
- TRIPS-plus provision and their social cost.
- Free Trade Agreements and typical TRIPS-plus clauses.
- The global landscape of IP regulation
- The Flexibilities of the TRIPS Agreement
- TRIPS-Plus rules
- Impact of TRIPS-Plus rules on medicines prices
- Limiting the impact of TRIPS-Plus rules
A Mutual Recognition Agreement for Pharma GMP InspectionsEMMAIntl
The European Medicines Agency (EMA) and the United States FDA have fully implemented the Mutual Recognition Agreement beginning July 11, 2019. This agreement allows the European member states and the FDA to rely on each other’s GMP inspections of pharmaceutical manufacturers...
Until the introduction of self-service around 1970, service station workers in the Nordic countries were exposed to gasoline vapors. Based on measurements reported in the literature, the 8-hour time-weighted average benzene exposure was estimated to be in the range of 0.5-1 mg/m3. 19,000 service station workers from Denmark, Norway, Sweden, and Finland were studied. Followed through 20 years, 1,300 cases of cancer were observed.
This presentation by the Turkish Competition Authority was made during a workshop on “Recent Challenges in Competition and IP in Pharmaceutical Markets” held by the OECD in Paris on 26 February 2019. More papers and presentations on the topic can be found out at oe.cd/2tD
This presentation by Italy was made during a workshop on “Recent Challenges in Competition and IP in Pharmaceutical Markets” held by the OECD in Paris on 26 February 2019. More papers and presentations on the topic can be found out at oe.cd/2tD
Medical Transparency: The Turkish CaseMeTApresents
Presentation by Şerif BOYACI, pharmacist, Turkish Pharmacists' Association on Medical Transparency: The Turkish Case, during the 69th FIP Congress, Istanbul, September 2009.
Swiss Doctors Can Now Prescribe Medical MarijuanaEvergreen Buzz
The Swiss go green, read this https://cannabis.net/blog/news/the-swiss-go-mmj-swiss-doctors-can-prescribe-medical-marijuana-without-exceptional-authorizatio
2010 and 2011 eu competition law and case law developments with a nexus to po...Michal
This third overview of EU competition and sector-specific regulatory jurisprudential
and case law developments with a nexus to Poland covers the years 2010 and 2011.
This period of time is worth noting for several reasons. First, EU courts delivered
a significant number of judgments in ‘Polish’ cases including an increased number of
preliminary rulings. Second, 2010-2011 developments were dominated by judgments
and decisions concerning telecoms. Finally, the Commission adopted only a handful
of Polish State aid decisions following a formal investigation procedure under
Article 108(2) TFEU.
Thomas Schael - Eye for Pharma Berlin 2013: A regional payers’ perspective of...Thomas Schael (PhD)
Thomas Schael's presentation on insights and actionables on drug expenditure and the requirements of Italian payers for market access at the Payers' Forum Europe 2013 in Berlin.Thomas Schael discusses Italy’s drug distribution system and explains how he dramatically cut spending on drugs. Schael gives his outlook on the major challenges for drug expenditure in Italy and Europe and offers advice to the pharmaceutical industry on how to work better with authorities.
Illegible prescription could lead to deficiency in serviceArunSharma10
Illegible prescription could lead to medical negligence and deficiency of service
Misinterpretation by the pharmacist
Wrongful dispensing of medicines by pharmacist
National Consumer Disputes Redressal Commission
Delhi State Consumer Disputes Redressal Commission
Consumer court
Medical negligence
Medical negligence in nephrology
Bad handwriting in prescription
Opportunities for Reform and Optimization presented by Mohammed El Said from the University of Central Lancashire (UCLAN) UK. Presentation includes:
- TRIPS-plus provision and their social cost.
- Free Trade Agreements and typical TRIPS-plus clauses.
- The global landscape of IP regulation
- The Flexibilities of the TRIPS Agreement
- TRIPS-Plus rules
- Impact of TRIPS-Plus rules on medicines prices
- Limiting the impact of TRIPS-Plus rules
A Mutual Recognition Agreement for Pharma GMP InspectionsEMMAIntl
The European Medicines Agency (EMA) and the United States FDA have fully implemented the Mutual Recognition Agreement beginning July 11, 2019. This agreement allows the European member states and the FDA to rely on each other’s GMP inspections of pharmaceutical manufacturers...
Until the introduction of self-service around 1970, service station workers in the Nordic countries were exposed to gasoline vapors. Based on measurements reported in the literature, the 8-hour time-weighted average benzene exposure was estimated to be in the range of 0.5-1 mg/m3. 19,000 service station workers from Denmark, Norway, Sweden, and Finland were studied. Followed through 20 years, 1,300 cases of cancer were observed.
This presentation by the Turkish Competition Authority was made during a workshop on “Recent Challenges in Competition and IP in Pharmaceutical Markets” held by the OECD in Paris on 26 February 2019. More papers and presentations on the topic can be found out at oe.cd/2tD
This presentation by Italy was made during a workshop on “Recent Challenges in Competition and IP in Pharmaceutical Markets” held by the OECD in Paris on 26 February 2019. More papers and presentations on the topic can be found out at oe.cd/2tD
Medical Transparency: The Turkish CaseMeTApresents
Presentation by Şerif BOYACI, pharmacist, Turkish Pharmacists' Association on Medical Transparency: The Turkish Case, during the 69th FIP Congress, Istanbul, September 2009.
Swiss Doctors Can Now Prescribe Medical MarijuanaEvergreen Buzz
The Swiss go green, read this https://cannabis.net/blog/news/the-swiss-go-mmj-swiss-doctors-can-prescribe-medical-marijuana-without-exceptional-authorizatio
How much THC can you put in food, read this https://cannabis.net/blog/news/how-much-thc-can-you-legally-eat-or-drink-the-eu-sets-the-standard-for-cannabisinfused-foods
Legal Limits Set for Cannabis-Infused FoodsCannabis News
How much cannabis can you put in food, read this https://cannabis.net/blog/news/how-much-thc-can-you-legally-eat-or-drink-the-eu-sets-the-standard-for-cannabisinfused-foods
Italian Supreme Court Stops Recreaional Marijuana LawsEvergreen Buzz
The Italian Supreme court stops marijuana legalization, read this https://cannabis.net/blog/news/fanculo-alla-corte-suprema-italys-supreme-court-strikes-down-recreational-marijuana
All eyes on pharmaceutical expenditures in the hospital sectorAxon Healthcare
Expensive hospital drugs have been the subject of a fierce public and political debate in The Netherlands for almost two years.
This whitepaper will delve deeper into this debate by providing an overview, relevant background information and a short analysis. This whitepaper will also explain which measures are being considered to curb pharmaceutical expenditures. These will likely focus on limiting open access in the hospital sector, stimulating the use of financial arrangements, and promoting joint procurement of medicines by small European countries.
Sfee press release_disclosure_code_20141009_2Market iT
EFPIA Member Association SFEE (The Hellenic Association of Pharmaceutical Companies) last week introduced a new code of industry self-regulation, in line with the EFPIA Disclosure Code
Is Weed Causing People to Leave Their Religion?Cannabis News
Religion and people using cannabis, read this https://cannabis.net/blog/opinion/the-great-exodus-from-organized-religion-is-cannabis-playing-a-key-role
Should We Put Social Justice and Cannabis Reform Together Anymore?Cannabis News
Is social justice and cannabis reform working, read this https://cannabis.net/blog/opinion/is-mixing-social-justice-with-marijuana-reform-doing-more-harm-than-good-right-now
Do Marijuana Users Need More Drugs During Endoscopies and Colonoscopies?Cannabis News
Yes, they do on MAC scores, read this https://cannabis.net/blog/medical/whats-your-mac-score-why-cannabis-users-need-stronger-sedation-drugs-for-colonoscopies-and-endo
Can the Cannabis Industry Lead the Way on Water Issues in the World?Cannabis News
The marijuana industry to the rescue, read this https://cannabis.net/blog/opinion/how-the-cannabis-industrys-technology-could-help-solve-the-worlds-water-problems
The Conscious Cannabis Consumer Through the Lens of Psychologist Ken WilberCannabis News
Yes, he can look at weed, read this https://cannabis.net/blog/opinion/the-stages-of-the-conscious-cannabis-consumer-through-the-lens-of-psychologist-ken-wilber
Did Evolution Happen Due to Apes Eating Magic Mushrooms?Cannabis News
The Stoned Ape Theory of Evolution explained, read this https://cannabis.net/blog/opinion/did-apes-evolve-into-humans-because-they-ate-magic-mushrooms-the-stoned-ape-theory-of-evolution
The history of marijuana and racism, read this https://cannabis.net/blog/opinion/if-you-think-the-word-marijuana-is-racist-does-that-make-you-a-racist-too
RMD24 | Debunking the non-endemic revenue myth Marvin Vacquier Droop | First ...BBPMedia1
Marvin neemt je in deze presentatie mee in de voordelen van non-endemic advertising op retail media netwerken. Hij brengt ook de uitdagingen in beeld die de markt op dit moment heeft op het gebied van retail media voor niet-leveranciers.
Retail media wordt gezien als het nieuwe advertising-medium en ook mediabureaus richten massaal retail media-afdelingen op. Merken die niet in de betreffende winkel liggen staan ook nog niet in de rij om op de retail media netwerken te adverteren. Marvin belicht de uitdagingen die er zijn om echt aansluiting te vinden op die markt van non-endemic advertising.
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Cracking the Workplace Discipline Code Main.pptxWorkforce Group
Cultivating and maintaining discipline within teams is a critical differentiator for successful organisations.
Forward-thinking leaders and business managers understand the impact that discipline has on organisational success. A disciplined workforce operates with clarity, focus, and a shared understanding of expectations, ultimately driving better results, optimising productivity, and facilitating seamless collaboration.
Although discipline is not a one-size-fits-all approach, it can help create a work environment that encourages personal growth and accountability rather than solely relying on punitive measures.
In this deck, you will learn the significance of workplace discipline for organisational success. You’ll also learn
• Four (4) workplace discipline methods you should consider
• The best and most practical approach to implementing workplace discipline.
• Three (3) key tips to maintain a disciplined workplace.
Memorandum Of Association Constitution of Company.pptseri bangash
www.seribangash.com
A Memorandum of Association (MOA) is a legal document that outlines the fundamental principles and objectives upon which a company operates. It serves as the company's charter or constitution and defines the scope of its activities. Here's a detailed note on the MOA:
Contents of Memorandum of Association:
Name Clause: This clause states the name of the company, which should end with words like "Limited" or "Ltd." for a public limited company and "Private Limited" or "Pvt. Ltd." for a private limited company.
https://seribangash.com/article-of-association-is-legal-doc-of-company/
Registered Office Clause: It specifies the location where the company's registered office is situated. This office is where all official communications and notices are sent.
Objective Clause: This clause delineates the main objectives for which the company is formed. It's important to define these objectives clearly, as the company cannot undertake activities beyond those mentioned in this clause.
www.seribangash.com
Liability Clause: It outlines the extent of liability of the company's members. In the case of companies limited by shares, the liability of members is limited to the amount unpaid on their shares. For companies limited by guarantee, members' liability is limited to the amount they undertake to contribute if the company is wound up.
https://seribangash.com/promotors-is-person-conceived-formation-company/
Capital Clause: This clause specifies the authorized capital of the company, i.e., the maximum amount of share capital the company is authorized to issue. It also mentions the division of this capital into shares and their respective nominal value.
Association Clause: It simply states that the subscribers wish to form a company and agree to become members of it, in accordance with the terms of the MOA.
Importance of Memorandum of Association:
Legal Requirement: The MOA is a legal requirement for the formation of a company. It must be filed with the Registrar of Companies during the incorporation process.
Constitutional Document: It serves as the company's constitutional document, defining its scope, powers, and limitations.
Protection of Members: It protects the interests of the company's members by clearly defining the objectives and limiting their liability.
External Communication: It provides clarity to external parties, such as investors, creditors, and regulatory authorities, regarding the company's objectives and powers.
https://seribangash.com/difference-public-and-private-company-law/
Binding Authority: The company and its members are bound by the provisions of the MOA. Any action taken beyond its scope may be considered ultra vires (beyond the powers) of the company and therefore void.
Amendment of MOA:
While the MOA lays down the company's fundamental principles, it is not entirely immutable. It can be amended, but only under specific circumstances and in compliance with legal procedures. Amendments typically require shareholder
Attending a job Interview for B1 and B2 Englsih learnersErika906060
It is a sample of an interview for a business english class for pre-intermediate and intermediate english students with emphasis on the speking ability.
3.0 Project 2_ Developing My Brand Identity Kit.pptxtanyjahb
A personal brand exploration presentation summarizes an individual's unique qualities and goals, covering strengths, values, passions, and target audience. It helps individuals understand what makes them stand out, their desired image, and how they aim to achieve it.
Enterprise Excellence is Inclusive Excellence.pdfKaiNexus
Enterprise excellence and inclusive excellence are closely linked, and real-world challenges have shown that both are essential to the success of any organization. To achieve enterprise excellence, organizations must focus on improving their operations and processes while creating an inclusive environment that engages everyone. In this interactive session, the facilitator will highlight commonly established business practices and how they limit our ability to engage everyone every day. More importantly, though, participants will likely gain increased awareness of what we can do differently to maximize enterprise excellence through deliberate inclusion.
What is Enterprise Excellence?
Enterprise Excellence is a holistic approach that's aimed at achieving world-class performance across all aspects of the organization.
What might I learn?
A way to engage all in creating Inclusive Excellence. Lessons from the US military and their parallels to the story of Harry Potter. How belt systems and CI teams can destroy inclusive practices. How leadership language invites people to the party. There are three things leaders can do to engage everyone every day: maximizing psychological safety to create environments where folks learn, contribute, and challenge the status quo.
Who might benefit? Anyone and everyone leading folks from the shop floor to top floor.
Dr. William Harvey is a seasoned Operations Leader with extensive experience in chemical processing, manufacturing, and operations management. At Michelman, he currently oversees multiple sites, leading teams in strategic planning and coaching/practicing continuous improvement. William is set to start his eighth year of teaching at the University of Cincinnati where he teaches marketing, finance, and management. William holds various certifications in change management, quality, leadership, operational excellence, team building, and DiSC, among others.
Unveiling the Secrets How Does Generative AI Work.pdfSam H
At its core, generative artificial intelligence relies on the concept of generative models, which serve as engines that churn out entirely new data resembling their training data. It is like a sculptor who has studied so many forms found in nature and then uses this knowledge to create sculptures from his imagination that have never been seen before anywhere else. If taken to cyberspace, gans work almost the same way.
Putting the SPARK into Virtual Training.pptxCynthia Clay
This 60-minute webinar, sponsored by Adobe, was delivered for the Training Mag Network. It explored the five elements of SPARK: Storytelling, Purpose, Action, Relationships, and Kudos. Knowing how to tell a well-structured story is key to building long-term memory. Stating a clear purpose that doesn't take away from the discovery learning process is critical. Ensuring that people move from theory to practical application is imperative. Creating strong social learning is the key to commitment and engagement. Validating and affirming participants' comments is the way to create a positive learning environment.
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[Note: This is a partial preview. To download this presentation, visit:
https://www.oeconsulting.com.sg/training-presentations]
Sustainability has become an increasingly critical topic as the world recognizes the need to protect our planet and its resources for future generations. Sustainability means meeting our current needs without compromising the ability of future generations to meet theirs. It involves long-term planning and consideration of the consequences of our actions. The goal is to create strategies that ensure the long-term viability of People, Planet, and Profit.
Leading companies such as Nike, Toyota, and Siemens are prioritizing sustainable innovation in their business models, setting an example for others to follow. In this Sustainability training presentation, you will learn key concepts, principles, and practices of sustainability applicable across industries. This training aims to create awareness and educate employees, senior executives, consultants, and other key stakeholders, including investors, policymakers, and supply chain partners, on the importance and implementation of sustainability.
LEARNING OBJECTIVES
1. Develop a comprehensive understanding of the fundamental principles and concepts that form the foundation of sustainability within corporate environments.
2. Explore the sustainability implementation model, focusing on effective measures and reporting strategies to track and communicate sustainability efforts.
3. Identify and define best practices and critical success factors essential for achieving sustainability goals within organizations.
CONTENTS
1. Introduction and Key Concepts of Sustainability
2. Principles and Practices of Sustainability
3. Measures and Reporting in Sustainability
4. Sustainability Implementation & Best Practices
To download the complete presentation, visit: https://www.oeconsulting.com.sg/training-presentations
Accpac to QuickBooks Conversion Navigating the Transition with Online Account...PaulBryant58
This article provides a comprehensive guide on how to
effectively manage the convert Accpac to QuickBooks , with a particular focus on utilizing online accounting services to streamline the process.
India Orthopedic Devices Market: Unlocking Growth Secrets, Trends and Develop...Kumar Satyam
According to TechSci Research report, “India Orthopedic Devices Market -Industry Size, Share, Trends, Competition Forecast & Opportunities, 2030”, the India Orthopedic Devices Market stood at USD 1,280.54 Million in 2024 and is anticipated to grow with a CAGR of 7.84% in the forecast period, 2026-2030F. The India Orthopedic Devices Market is being driven by several factors. The most prominent ones include an increase in the elderly population, who are more prone to orthopedic conditions such as osteoporosis and arthritis. Moreover, the rise in sports injuries and road accidents are also contributing to the demand for orthopedic devices. Advances in technology and the introduction of innovative implants and prosthetics have further propelled the market growth. Additionally, government initiatives aimed at improving healthcare infrastructure and the increasing prevalence of lifestyle diseases have led to an upward trend in orthopedic surgeries, thereby fueling the market demand for these devices.
India Orthopedic Devices Market: Unlocking Growth Secrets, Trends and Develop...
The European Marijuana Business News Report
1. 8/1/2020 The European Weed Report
https://cannabis.net/blog/news/the-european-weed-report 2/14
EUROPEAN WEED REPORT
h d
2. 8/1/2020 The European Weed Report
https://cannabis.net/blog/news/the-european-weed-report 4/14
Currently, Switzerland allows its citizens to consume low potency cannabis, but for the most part, the drug is banned for
recreational use. However, it looks like this may change sometime soon.
The Swiss government is allowing pilot studies to help them determine the best way to legalize their laws, while making
it easier for patients to access cannabis to treat conditions such as cancer or multiple sclerosis. Around 200,000 people
in Switzerland currently consume cannabis recreationally.
“Although current laws forbid its consumption and seek to punish it, this number is not declining,” the Swiss
government says. “At the same time, the black market is ourishing, and the safety of consumers cannot be guaranteed
due to a lack of quality control.”
A number of cities and cantons throughout the country want to participate in studies to best determine a regulation
model that will work for them, says a statement from the Federal Council. The statement also called for changes to
allow the studies to be legally conducted.
3. 8/1/2020 The European Weed Report
https://cannabis.net/blog/news/the-european-weed-report 3/14
The European Weed Report
Swiss Go Green, Luxembourg Goes MMJ, Israel Shows Up
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HighChi on Tuesday Jul 10, 2018
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Switzerland Considers Relaxing Cannabis Laws
4. 8/1/2020 The European Weed Report
https://cannabis.net/blog/news/the-european-weed-report 5/14
“The scienti c pilot studies would be limited and restricted to speci c areas,” says the government. “Participant numbers
would also be limited, and minors would be excluded.” The consultations on the proposed pilot studies will go on until
October 25, and interested parties can send in their comments during this time.
For Swiss medical cannabis patients, the law requires them to ask for approval from the federal health ministry, which
the government says makes it harder for the 3,000 patients who use the drug to access it at all. The government asked
the Swiss Interior Ministry to draft a proposal that will be ready next summer which would iron out the process, and it’s
up to the Health Ministry to determine how insurance will work in the grand scheme of things.
Luxembourg Becomes Latest European Country To Legalize MMJ
Lawmakers in Luxembourg have collectively decided to support a bill that would legalize medical cannabis. The bill,
which was passed on June 28, now allows the drug to be prescribed and consumed by patients su ering from
chemotherapy-induced nausea, chronic pain, and muscle spasms caused by multiple sclerosis.
Although the original draft of the law says that only specialists would be legally allowed to prescribe cannabis, in the
nal version it states that general practitioners can prescribe it as long as they have undergone training.
Health Minister Lydia Mutsch commended (http://www.sante.public.lu/fr/actualites/2018/06/cannabis-
medical/index.html) the legislative support for the law. “I am pleased that the House has agreed with the bill to legalize
access to cannabis for medical purposes,” she says. “The medical use of cannabis is an important step in our e orts to
reduce the pain and su ering of some patients, where usual treatments do not allow it.”
Luxembourg will be importing their medical cannabis products from Canada.
It’s been a long way for Luxembourg, whose MMJ laws have been criticized in the past for being too strict. Some
lawmakers are worried that because only 4 hospitals will be giving access to cannabis, those living in the rural areas will
face di culties obtaining their medicine.
Red Tape Prompts Israel MMJ Growers To Set Foot In Europe
5. 8/1/2020 The European Weed Report
https://cannabis.net/blog/news/the-european-weed-report 7/14
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One of Israel’s newest cannabis growers is setting up shop in Europe. Together Pharma has just announced that some
of their greenhouse operations will be moved to a country in the EU, although it still hasn’t been announced where
exactly.
Israeli’s medical cannabis industry is facing problems caused by bureaucracy and red tape, combined with a failure to
legalize laws that would allow local growers to export cannabis to mature markets abroad. These issues have left Israeli
companies with no choice but to explore options abroad.
Although Israeli regulators said that they would permit cannabis exports this year, without the export regulations in
place, growers who have invested in cultivation sites may end up with nothing. “The delays a ect the money and the
business,” says Nir Sosinky, Together Pharma’s managing director. “We don’t know what the government policy is – we
can only guess,” he told the Jerusalem Post. (https://www.jpost.com/Israel-News/Israeli-medical-marijuana-grower-to-
shift-to-the-EU-amid-red-tape-561291)
Israel’s Public Security Ministry is facing scrutiny for the delays, which, if continued, could mean that other growers may
follow suit abroad.
Together Pharma has already signed a contract with a European Union country where they intend to build a 30,000
square foot facility, reports the Jerusalem Post.
The European Cannabis Report (https://vimeo.com/301192971) from CannabisNet (https://vimeo.com/user84347733)
on Vimeo (https://vimeo.com).
7. 8/1/2020 The European Weed Report
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biggest-cannabis-market-in-the-world)
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