Warung Bebas

Senin, 22 Juli 2013

Penggolongan Hukum

Para ahli hukum mengalami kesulitan pada saat membuat pengertian hukum yang singkat dan meliputi berbagai hal. Ini dikarenakan kompleksnya hukum yang berlaku dalam suatu Negara. Untuk memudahkan dalam membedakan hukum yang satu dengan yang lainnya, C.S.T. Kansil, membuat penggolongan hukum seperti berikut :
1. Menurut Sumbernya :
  • Hukum undang-undang; yaitu hukum yang tercantum dalam peraturan perundang-undangan.
  • Hukum kebiasaan (adat); yaitu hukum yang terletak di dalam peraturan-peraturan kebiasaan (adat)
  • Hukum traktat (perjanjian), yaitu hukum yang ditetapkan oleh Negara-negara dalam suatu perjanjian antar Negara.
  • Hukum Yurisprudensi; yaitu hukum yang terbentuk karena keputusan hakim.
2. Menurut Bentuknya :
  • Hukum Tertulis; hukum yang dicantumkan dalam berbagai peraturan.
  • Hukum Tidak Tertulis; hukum yang masih hidup dalam keyakinan masyarakat, tetapi tidak tertulis, namun berlakunya ditaati seperti suatu peraturan perundangan. Hukum tidak tertulis disebut juga sebagai suatu kebiasaan.
3. Menurut Tempat Berlakunya (ruang) :
  • Hukum Nasional; hukum yang berlaku dalam suatu Negara.
  • Hukum Internasional; hukum yang mengatur hubungan hukum dalam dunia internasional.
  • Hukum Gereja; kumpulan norma-norma yang ditetapkan.
  • Hukum Asing; hukum yang berlaku dalam Negara lain.
4. Menurut Waktu Berlakunya :
  • Ius Constitutium (Hukum positif/berlaku sekarang); hukum yang berlaku sekarang bagi masyarakat tertentu dalam suatu daerah tertentu (hukum yang berlaku dalam masyarakat pada suatu waktu, dalam suatu tempat tertentu).
  • Ius Constituendum (berlaku masa lalu); hukum yang diharapkan berlaku pada waktu yang akan datang.
  • Antar Waktu (hukum asasi/hukum alam); hukum yang berlaku dimana-mana dalam segala waktu dan untuk segala bangsa di dunia. Hukum ini tak mengenal batas waktu melainkan berlaku untuk selama-lamanya (abadi) terhadap siapapun juga di seluruh tempat.
5. Menurut Cara Mempertahankannya (Tugas & Fungsi) :
  • Hukum Materil (KUH Perdata, KUH Pidana, KUH Dagang).
  • Hukum Formal (Pidana Formal, Perdata Formal).
6. Menurut Sifatnya :
  • Hukum Memakasa (imperative); hukum yang dalam keadaan bagaimana pun juga harus dan mempunyai paksaan mutlak.
  • Hukum Mengatur (fakultatif/pelengkap); hukum yang dapat dikesampingkan apabila pihak-pihak yang bersangkutan telah membuat peraturan sendiri dalam suatu perjanjian.
7. Menurut Isinya :
  • Hukum Privat/Perdata (hukum pribadi, hukum kekayaan, hukum waris)
  • Hukum Publik (Hukum tata Negara, hukum administrasi Negara, hukum pidana, hukum acara, hukum internasional)
8. Menurut Pribadi :
  • Hukum Satu Golongan
  • Hukum Semua Golongan
  • Hukum Antar Golongan.
9. Menurut Wujudnya :
  • Hukum Objektif; hukum dalam suatu Negara yang berlaku umum dan tidak mengenai orang atau golongan tertentu.
  • Hukum Subjektif; Hukum yang timbul dari hukum objektif dan berlaku terhadap seorang tertentu atau lebih. Hukum subjektif disebut juga hak.
Baca juga selengkapnya tentang > SISTEM HUKUM INDONESIA

Pharmaceutical Industry "'Mobilised' an Army of Patient Groups to Lobby Against" Improving Clinical Research Integrity

I had guessed that this sort of thing was going on all the time, but being kept very well hidden.  Now we have some more evidence.

An article in yesterdays Guardian showed how the pharmaceutical industry is using pet patient advocacy groups in a public relations campaign to defeat calls for for measures against suppression and manipulation of clinical research. In summary,

The pharmaceutical industry has 'mobilised' an army of patient groups to lobby against plans to force companies to publish secret documents on drugs trials.

More specifically,


The strategy was drawn up by two large trade groups, the Pharmaceutical Research and Manufacturers of America (PhRMA) and the European Federation of Pharmaceutical Industries and Associations (EFPIA), and outlined in a memo to senior industry figures this month, according to an email seen by the Guardian.  The memo, from Richard Bergström, director general of EFPIA, went to directors and legal counsel at Roche, Merck, Pfizer, GSK, AstraZeneca, Eli Lilly, Novartis and many smaller companies. It was leaked by a drugs company employee.

The email describes a four-pronged campaign that starts with 'mobilising patient groups to express concern about the risk to public health by non-scientific re-use of data'. Translated, that means patient groups go into bat for the industry by raising fears that if full results from drug trials are published, the information might be misinterpreted and cause a health scare.

The lobbying is targeted at Europe where the European Medicines Agency (EMA) wants to publish all of the clinical study reports that companies have filed, and where negotiations around the clinical trials directive could force drug companies to publish all clinical trial results in a public database.

The argument for continuing to allow clinical trials to be suppressed was to be,

The patient groups focus on the concern that if companies release all of their clinical trials data, the information might be misconstrued, or intentionally cherry-picked, and spark damaging health scares around certain drugs or vaccines.

The Guardian story did not disclose which patient groups were cooperating with this effort.

By the way, the other parts of this strategy involved using scientific associations and academics to push the pharmaceutical companies' agenda,

 Two other strands of the campaign include discussions with scientific associations about the risks of data sharing, and work with other businesses that are concerned about the release of trade secrets and confidential data. The final strand calls, in the long term, for a network of academics across Europe that can be called on to correct false interpretations of the data. 
Several of the large multinational drug companies contacted by the Guardian issued the usual non-denial denials

In response to queries from the Guardian, GSK said: 'This is not something we are doing. One of the reasons we're involved in this is we want more companies to move towards greater transparency. I don't think it's for us to be mobilising patient groups to campaign on a negative level.'

A Roche spokesperson said the company consulted patient groups to understand their concerns about clinical trials, but 'to our knowledge Roche has not been involved in any EFPIA's potential activity in mobilising patient groups to express concern about the risk to public health by non-scientific re-use of data'.

A Lilly spokesman said: 'Lilly is committed to working with Europe-based patient advocacy organisations for the benefit of patients in a way that is true to the EFPIA code of practice and Lilly's integrity in business policy.'


Summary

We have long discussed and decried how vested interests, chiefly health care corporations with services and products to sell, have manipulated clinical research to make their wares look better, and suppressed research whose results, even if manipulated, could not be made sufficiently favorable. This has resulted in making drugs and devices look more efficacious and/or less hazardous than they really are.  See this post for our latest discussion, and information on the latest effort to counter suppression and manipulation of clinical research.

It is not surprising that pharmaceutical companies do not want to have to publish every clinical trial they sponsor, or expose their manipulations of these trials.  Instead, the Guardian article suggests that companies and their trade associations, including the US based pharmaceutical trade association, and several large US companies, and well as large companies based elsewhere, are using a third-party public relations strategy.  Wendell Potter's muckraking book on the US commercial health care insurance industry, Deadly Spin, revealed how similar strategies were used by US based health insurance companies to defeat the Clinton administration's attempt at health care reform, and other measures targeted to make the US commercial health care insurance system more equitable and ethical  (see post here).  Third party strategies are fundamentally deceptive.   

The current alleged use of the third party strategies by pharmaceutical companies to support ongoing suppression and manipulation of clinical research is more than just deceptive.  It is corrupt.

Patient advocacy groups are usually believed to represent patients' interests.  For such groups to support a public relations campaign that could allow ongoing harm of patients (by suppressing and manipulating evidence to prevent it from being used to forestall excess use of ineffective, dangerous drugs) is abuse of their entrusted power.  To do it for money, money used to support these groups, or help underwrite generous compensation for their executives, fits the definition of corruption used by Transparency International - abuse of entrusted power for private gain.

Note that the Guardian provided this viewpoint,

Tim Reed, of Health Action International, a group that has previously exposed the pharmaceutical industry's financial links with patient groups, said: 'It's incredibly ironic that this is a transparency initiative and we've now got clear indications that the pharmaceutical industry is ready to use patient organisations to fight their corner.

'It underlines the fact that patient groups who are in the pay of the pharmaceutical industry will go into battle for them. There's a hidden agenda here. The patient groups will say they think it's a great idea to keep clinical trials data secret. Why would they do that? They would do that because they are fronts for the pharmaceutical industry.

'Patient groups get traction because they are assumed to represent the voice of the suffering. But industry uses them to say we're not going to get innovative medicines if the industry is deterred from investing by having to be transparent about their clinical trials,' he added.

We have previously noted isolated examples of evidence that particular US based patient advocacy groups were being supported by commercial firms presumably to aid their marketing.  We have also found examples of conflicts of interest affecting medical societies, and many affecting non-profit hospitals and academic medical institutions, and their staff and faculty.  I begin to wonder if most health care non-profit organizations in the US, and now it appears maybe in UK and in Europe, have been paid off to support marketing and/or public relations interests of health care corporations.

This latest example suggests that health care worldwide has become deeply corrupt, even more corrupt than Transparency International's Global Report on health care corruption in 2006, or the those responding to Transparency International's global corruption survey in 2013, could envision.

I only hope that the pile up of new examples - each seemingly worse than the one before - of health care corruption, will be sufficient to overcome the anechoic effect, and create enough global outrage to give us a chance to clean up our corrupt health care before it destroys our health.

ADDENDUM (25 July, 2013) - See also comments by Dr Howard Brody on the Hooked: Ethics, Medicine and Pharma blog. 

ADDENDUM (29 July, 2013 - See the comment on the 1BoringOldMan blog. 

Kenangan Lama Bersamamu Membekas di Hati

Kenangan Lama Bersamamu Membekas di Hati - yoshiwafa - Inilah takdirku mengarungi harunya hidup tanpamu, tanpa belaian kasihmu, tanpa cintamu, tanpa senyumanmu, tanpa semuanya yang ada pada dirimu, dan hanya aku seorang diri bertemankan suyinya hari yang ku lewati tanpa adanya kau lagi. Tak seindah dulu, tak berwarna lagi seperti dahulu, sekarang hanya hitam dan putih dalam hidupku, tanpa

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