Impotentie brengt een constant ongemak met zich mee, net als fysieke en psychologische problemen in uw leven cialis kopen terwijl generieke medicijnen al bewezen en geperfectioneerd zijn
Pharmaceutical & Personal Care Products (PPCPs):
Modern society uses products that contain various chemicals for a wide variety of personal health and hygiene uses, including preventing and combating disease, alleviating symptoms from illness and injury, personal comfort, grooming and cosmetic purposes. Pharmaceutical and Personal Care Products (PPCPs) include medicines, insect repellents, sunscreens, perfumes, soaps, fragrances, and lotions. These products, which can be found in any drug store, have the potential to enter the environment through domestic sewage and other sources. Some are endocrine disrupting compounds (or EDCs) and could possibly affect the system of glands that produces hormones that help control the body's metabolic activity and development. The
Pain medications (Codeine, Vicodin, Percodan)
HOW PHARMACEUTICALS SHOULD BE STORED AND TRANSPORTED
conditions for pharmaceutical products and materials should be in compliance with the
labeling, which is based on the results of stability testing
Recorded temperature monitoring data should be available for review. The equipment used for
monitoring should be checked at suitable predetermined intervals and the results of such
checks should be recorded and retained. All monitoring records should be kept for at least the
shelf-life of the stored material or product plus 1 year, or as required by national legislation.
Temperature mapping should show uniformity of the temperature across the storage facility. It
is recommended that temperature monitors be located in areas that are most likely to show
Written instructions and records should be available which document all activities in the
storage areas including the handling of expired stock. These should adequately describe the
storage procedures and define the route of materials and pharmaceutical products and
information through the organization in the event of a product recall being required.
Permanent information, written or electronic, should exist for each stored material or product
indicating recommended storage conditions, any precautions to be observed and retest dates.
Pharmacopoeial requirements and current national regulations concerning labels and
containers should be respected at all times
Records should be kept for each delivery. They should include the description of the goods,
quality, quantity, supplier, supplier’s batch number, the date of receipt, assigned batch number
and the expiry date. Where national regulations prescribe that records must be retained for a
certain period, this must be observed. (Otherwise such records should be retained for a period
equal to the shelf-life of the incoming materials and products, where applicable, plus 1 year).
Materials and pharmaceutical products should be transported in such a way that their integrity
is not impaired and that storage conditions are maintained
Special care should be exercised when using dry ice in cold chains.
In addition observing to safety precautions, it must be ensured that the materials or product
does not come in into contact with dry ice, as this may adversely affect the product quality, e.g.
Where appropriate, the use of devices to monitor conditions such as temperature during
transportation is recommended. Monitoring records should be available for review.
The outside container should offer adequate protection from all external influences and should
be indelibly and clearly labeled http://apps.who.int/prequal/info_general/documents/TRS908/WHO_TRS_908-Annex9.pdf
Key requirements generally include ensuring that goods are appropriately classified, packaged and labelled. It is also important that everyone involved understands how to minimise risks. Special training may be required.
Decision The hospital, district or regional pharmacist or organizations with pharmaceutical programmes decide when action needs to be initiated, because of an accumulation of unwanted pharmaceuticals which are unfit for human consumption and for veterinary treatment. Approval Approval and sanctioning of disposal of pharmaceuticals must be sought from the appropriate authority. This authority will differ from country to country and may be the department responsible for pharmaceutical management within the ministry of health, the drug regulatory authority, or the regional or local health authority (pharmaceutical officer). In some countries the ministry of the environment should be involved. The guidelines are particularly useful in emergency situations or for countries in transition where official regulations have not yet been developed. In non-emergency situations when significant quantities of donated pharmaceuticals are disposed of, for whatever reason, it may be necessary and judicious to inform the donor. Planning Planning, in terms of funding, necessary expertise, human resources, professional time, space, equipment, material and available disposal options will be required. This is essential before practical steps can be taken to start disposal. To obtain a rough estimate of the volume of materials to be sorted, it is recommended that measurements are made using a tape measure, and conversion from volume of material to weight is made using a density figure of 0.2 metric tons/cubic metre. Forming work teams Work should be conducted by teams consisting of supervising pharmacists and general medical workers, who are preferably pharmaceutical technicians or experienced pharmaceutical warehouse personnel. The size of each team, and the ratio of experts to workers, will be determined by the volume and composition of the stockpiles, and working conditions at the sites. Health and safety of work teams All workers should wear appropriate protective equipment including overalls and boots at all times, and gloves, masks and caps when appropriate. Masks should be worn when tablets or capsules are being crushed as part of the disposal technique (for example, inertization, and see Section 2.4) and when there is a risk of powders being liberated. Particular care is required when handling antineoplastics.
The objective of sorting is to separate the pharmaceuticals into separate categories for which
different disposal methods are required. The separation should be made into those that can be
safely used and returned to the pharmaceutical supply system and those that require disposal
by different methods. For example, controlled drugs (e.g. narcotics), antineoplastic drugs and
antibiotics all require special methods of disposal. Substantial investment in human resources
may be required for identifying and separating pharmaceuticals.
Disposal options vary considerably between situations, and the ideal solution may not be
feasible. The aim of these guidelines is to propose the simplest, safest and most practical
Controlled substances (e.g. narcotics and psychotropics) require tight security and control. In
some countries, scavenging of material from landfills is a frequent problem, and, disposed
drugs may be recovered and sold by the scavengers. Measures are therefore necessary to
prevent diversion during sorting, and pilfering of drugs from landfills. Immobilization (see
Sections 2.3 and 2.4) is the best method of preventing pilfering from a store or landfill. If, as a
last resort, pharmaceuticals must be discarded direct to a landfill then they must be covered
immediately with a large quantity of municipal waste. http://www.who.int/water_sanitation_health/medicalwaste/unwantpharm.pdf
Sewage treatment plant (STP) effluents, Surface waters, Seawater, groundwater and even drinking water.
See also: http://phys.org/news/2010-10-environmental-pharmaceuticals-inadequate.html
November 2009 - 11 月 Ambassador's Message Ａs Autumn comes round again the November edition of the Embassy newsletter brings you the latest information on the Ireland Japan Chamber of Commerce, Japan GAA and a variety of upcoming Ireland-related events on the calendar. I am particularly pleased to announce the signing of a bilateral Social Security Agreement between Ireland and
Symposium on food security and biodiversity: Benefit sharing Case Study: San/CSIR Hoodia Benefit Sharing Petro Terblanche Executive Director Bio/Chemtek, Council for Scientific and Industrial benefits from bioprospecting with the owners of the traditional knowledge that led to its initial discovery. In 1998, Phytopharm sold the rights to the compound, now known as P57, to pharmaceut