PHARMA GUIDE

How to apply for DHA? Latest info... -  The pharmacists have to apply online Pharmacist fall in Allied Health category, initially the online application will be reviewed (takes approximately 15 days). -   Create DHA (Sheryan Account), Go to https://eservices.dha.gov.ae/DHAWeb/Default.aspx. Click New User Registration and after filling profile click Create User. There is no Fee for this. -  Login in to your DHA account, click for Individual/Individual Home and then click Health Licensing Services then go to New Professional License. At first they will ask you to fill online Application form, select Allied Health in “I am looking for field” and complete remaining profile. Upload required scanned documents to your DHA Account: The documents to be upload are 1- PASSPORT 2- RECENT PICTURE 3- DEGREE (Pharm D/ Pharm B) 4- TRANSCRIPT RELATED TO THE DEGREE 5- GOOD STANDING CERTIFICATE     *(This certificate u can get from pharmacy council of your home country from where u studied Ph

·          Here we are discussing about important, role and posts of Regulatory Affairs. ·          Regulatory Affairs used to protect public health from the medicines. ·          IMPORTANTS OF REGULATORY AFFAIRS: ·          Identification of various regulatory options for drug development. ·          Optimising the products. ·          Speeding it means Time to Market strategic thinking. ·          Involvement in critical business functions. ·          Engagement in manufacturing site optimisation activities. ·          Regulatory expertise throughout the product lifecycle. ·          ROLE OF REGULATORY AFFAIRS: ·          Central involvement in development process. ·          Construction of core dossier (documentation). ·          Involvement in data management. ·          Local SOP’S control ·          Focus on complains (QA, GMP, CGMP). ·          Involvement in site inspections. ·          Involvement in audits. ·          Involvement in c

Here we are discussing about role of Kuwait pharmacist in hospitals. Initially we have to send request for medicine to the central medical store. These request are three types those are 1. normal request                                      2. special request                                      3. urgent request. After that we receive the stock and it will arrange alphabetically. Then we should register the stock as per our indent. And handling of prescription for the out patients. handling of discharge the patients. Preparation of in-patients prescriptions. Supply of ward stock and other pharmacy requests. We have to do daily stock check in the morning. At the same time we have to check expiry medicines properly. Follow 365 circular drugs process. Maintain unit dose management system. We have to do filling and labeling. In these filling three types of methods are involved, those are capsule filling, Vaseline filling and labeling.

We are discussing about Batch Production Control Record check list. The BPCR review should cover and typically requires the reviewer to initial each section that has been reviewed. A specific check list should be prepared for each type of finished drug product because the manufacture of tablets, capsules and oral liquids vary by process and parameters. The important check points are mentioned here, those are * Check for total number of pages. * Check for batch numbers on all pages. * Check for issued signature. * Check whether all the columns are filled properly. * Check for over writings. * Check for QC reference numbers for all the raw materials. * Check the dispencing labels ate attached and filled completely. * Check all the parameters like temperature, pressure are recorded as per BPCR. * Check all the in process samples sent to QC as per BPCR. * Check the Yield column filled. * Is there any Deviation related to this batch, wether the deviation is clos

We are discussing about ICH Guidelines part-2. The International Conference on Hormonisation of techinical requirments for registration of pharmaceuticals for human use. Since its inception in 1990, ICH has gradually evolved to respond to the incresingly global face of drug development. The ICH guidelines are explained in 4 different topics, those are 1.Quality topics           2.Safety topics           3.Efficacy topics           4.Multi disciplinary topics. The work carried out by ICH under the Efficacy heading is concerned with design, conduct, safety and reporting of clinical trials. The clinical trials are two types, those are pre-clinical trials and clinical trails. The pre-clinical trials are carried throughout the animals, after its succeed it will entered in human body and it is commonly called as clinical trials. It is also covers novel types of medicines derived from biotechnological processes and the use of pharmacogenetics or pharmacogenomics techniques

We are discussing about ICH Guidelines. The International Conference on Hormonisation of techinical requirments for registration of pharmaceuticals for human use. Since its inception in 1990, ICH has gradually evolved to respond to the incresingly global face of drug development. The ICH guidelines are explained in 4 different topics, those are                                                                   1.Quality topics           2.Safety topics           3.Efficacy topics           4.Multi disciplinary topics. Hormonisation achievements in the quality area include pivotal milestsones such as the conduct of stability studies. In Quality topics, stability is one of the most important topic, in this 3 different types of stabilities are involved. Those are Long term stability, accelarated stability and intermediate stability. In this impurity testing 3 types of impurities are checked,those are Organic impurities, Inorganic impurities and Residual impurities. The

Here we are discussing about Pharmaceutical Analysis job opportunities. we have number of opportunities in Research and Development department. At the same time Analytical R&D also gives no.of opportunities. In Production department three types of jobs are providing for Analysis students, those are         1.Formulation Development Department.         2.Active Pharmaceutical Ingredient Development Department.         3.Bulk Development Department. And also number of opportunities in Quality Control Department. At the same time Quality Assurance also providing no.of job opportunities for Analysis students. The Regulatory Affairs department having different posts like Public health officers and Health proffessional officers. The Pharma covigilence department was giving good opportunities for analysis students. In Business side number of ways are available for analysis students like, sales and marketing, product analyzer, management and product trainer. The Medi

• Here we are discussing about good manufacturing practices. • A GMP is a system for ensuring that products are consistently produced and controlled according to quality standards. • GMP designed to minimise the risks involved in any pharmaceutical production, that cannot be eliminated through testing the final product. • Some of the rules and regulations of GMP are, • Writing step by step Standard Operating Procedures and work instructions. • Then following written procedures and instructions. • Documenting our work. • Validating our work. • Designing and constructing facilities and equipment. • Protecting against contamination. • Controlling components and product related processes. • Conducting planned and periodic audits.

• We are discussing about Validation process in pharma industry. • Validation is the process of establishing documentary evidence. • It is demonstrating that a procedure, process or activity carried out in testing. • And then production maintains the desired level of compliance at all stages. • The validation is involved four types of processes, those are • 1. Analytical method validation • 2. Equipment validation • 3. Process validation • 4. Cleaning validation • These validations are used for different types of methods, some of them are • We can calculate the accurate values in this validation process. • By using this validation, we can find the precision values. • The validation process is used for to specify the products. • It is used for to detect the limit of product. • We can calculate the limit of quantitation. • By using this validation process, we can fix the linearity and range of the product.

• We are discussing about Pharmaco vigilance briefly. • The history of Pharmaco vigilance also observed clearly. • The Regulatory authorities also involved in this video. • And clearly discussed the clinical trials, pre-clinical trials. • The Pharmaco vigilance officers are responsible for the monitoring and reporting the effectiveness and any adverse effects or side effects of pharmaceutical products on the market. • Recording and reporting adverse reactions from health care professionals and consumers. • Conducting depth interviews with patients and health care professionals. • Developing thorough knowledge of products. • Collecting periodic safety update reports form the respective companies. • Writing and reviewing of serious adverse effects. • The safety audits to be conducted yearly. • Minimising the risk of serious side effects. • Working on clinical trials of new drugs. • They are liable with medical representatives, patients, doctors and other health

Here we are discussing about pharmacology job features for freshers. for more details follow https://youtu.be/yaaKoIzvzFE for Quality Control reference https://youtu.be/wjpCn3g8TZk for R&D reference https://youtu.be/ZDCtkT0bQ7I for more details follow me on youtube UCxGjNIWjjz85nBadgB7_tyw

•We are discussing about b.pharmacy further education. • After b.pharmacy we have to enter in p.g course like different branches. • Pharmaceutics is one of the best branch in M.pharma studies. • In this m.pharma studies Quality assurance play an important role. • And one more medicinal chemistry also involved in the m.pharmacy. • The Pharmacology studies also occurred in post-graduation. • The Pharmacology is a typical department in the m.pharmacy studies. • In this m.pharmacy Novel drug delivery system Is one of the best department. • The industrial pharmacy also established in the post-graduation. • The Forensic pharmacy is very tough subject in the m.pharma studies. • After b.pharmacy, the best choice is patent laws, it is mainly involved in Intellectual property rights. • And one more option is Management, in these MBA, and PGDM (post-graduation development management) are most important departments. • After graduation, we will go the clinical research like

• Here we are discussing about Patient rights in hospitals. • Right to information: you have the right to receive information about the name and qualification of your treating doctor, your state of health, possible complications and its prevention, approximate cost of treatment, treatment plan, use of medications, diet and nutrition and how to voice your complaint. • Right to consent: you have the right to give or withhold your consent for any proposed care. You have a right to seek a second medical option before giving the consent. You have the right to refuse consent before intimation of clinical research. • Right to choose: you have the right to know all your treatment options and to participate in decisions about your care. • Right to privacy: you have the right to receive reasonable privacy during consultation or examination or treatment and various investigative procedures. You have the right to your health information protected. • Right to respect: you have the right t

 • We are discussing about Hospital Codes or Emergency Codes. • These Emergency codes are used to intimate the emergency conditions into the hospitals. • Code red is used for to identify the Fire conditions in the hospitals surroundings. • Code blue is used for to identify any medical emergency for the patients. • Code pink is used for to identify the child abduction (missing) in the hospitals. • Code black is used for to identify the bomb threat in the hospitals. • Code orange is used for to identify the hazardous materials in the hospital surroundings. • Code green is used for to identify the violent behavior from the patient or patient attender. • Code grey is used for to identify the disaster either internal or external surroundings of the hospitals. • Code white is used for to identify the pediatric emergency or child emergency. • Code silver is used for to identify the controlled access its means person with a weapon.

 we are discussing the budget of hospital pharmacy. • OP Sale: It is out-patient pharmacy sale, we have count both card sale and cash sale. • OP Return's: some of the o.p patients, they will return the medicines, so this is considered as an o.p returns. • IP Issues: It is in-patient pharmacy sale, this total bill will collect before patient discharge from the hospital. • IP Return's: Some of the i.p patients, they will return the medicines, so this is considered as an i.p returns. • Discounts: some patients are having health insurance or senior citizen health cards, so in this situation, we are considered as discounts. • Purchase: some of lacking items we are getting from vendors, so the vendors are sending the items through the goods receipt note, based on these we are observing the total amount of purchased rate. • Dialysis: The dialysis patients are daily visitors to the hospital because they have to check their health conditions daily on the basis of dialysis.

 we are discussing about Out Patient Pharmacist role in hospital pharmacy. • The initial role of O.P pharmacist is handling of prescriptions. • Carefully dispense the medicines with prescription. • And neatly pack the medicines with separate covers. • And give the proper guidance to the patient how to take. • Carefully observe the LASA (Look a like, Sound a like) drugs. • Must and should follow the FIFO (First in First order) order. • Maintain proper expiry drugs in the pharmacy. • Special care about Scheduled drugs like narcotics. • Generally OP pharmacist well known about patient rights. • OP Pharmacist should be follow the hospital policies and values. • OP Pharmacist should be follow the hospital mission and vision. • Monitoring the temperature sheets of refrigerator. • Checking for any medication errors in the prescriptions. • Checking the storage conditions of medicines in the pharmacy. • Stock checking should be done in every month of ending. • An

 we are discussing about IP PHARMACIST role in hospital. • Handling of prescriptions from the ward. • Initially we have to check and prepare ward stock for in patients. • Well known about Posology studies. • Checking for any medication errors in the IP prescriptions. • Checking the storage conditions of medicines in wards. • Providing drug information for the medical staff in the ward. • Co-ordination with senior pharmacist to ordering or purchasing any unavailable medicines from the other hospitals or other pharmacies. • Reporting to the chief pharmacist about ward visits. • Receiving and checking the returned medicines from the wards. • Update the ward stocks every month.

 we are discussing how to use Personal Protective Equipments in the plant. • Mainly must and should we have to wear Helmet for head protection in the plant. • We have to use Goggles for eye safety protection in the plant. • We are using different types of Masks those are with loop type and with tie type. • For hands safety we are using different types of Gloves those are rubbered gloves and latex gloves. • The Aprons are mainly used for our safety purpose, each department has different types of colored indicated aprons. • The maintenance department has Green colored apron, and electrical department having Blue colored apron. • The Shoes are used for legs protections, these are electric proof-oriented shoes. • The napkins are used for cleaning purpose, and these are industrially called as lint-free cloth. • Every weekend we are must and should eat jaggery. It is useful to dissolve chemical foams and smoke. • In this plant, mobiles are strictly prohibited. • At the

• In this stores department we are collecting raw material from the vendor. • Then it will send to the Quality control department to sample test. • The finished products are kept under separate section, and these are ready to sending out through the distributors. • The indents are requesting from the all departments like Production, Quality control, Quality assurance, and R & D departments. • In this ware house different types of labels are available, those are • Approved labels:  these are in green colour label. • To be tested:  these are in orange colour label. • Rejected labels:  these are in red colour label. • In these store department, each raw material having their individual code numbers. • The raw material and finished products are stored in well containers and calibrated refrigerators. • In these ware house department, we are using different types of equipment’s those are • Weighing balances, refrigerators, drums, carbyles, trollies, glassware’s, lab

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It's my Blogger introduction. How to get Pharma Job  Govt sector or private sector, How to fulfill Interview phobia, How to behave with consultancies, How to get Abroad Jobs, How to write entrance exams like MOH, DHA, HAAD, PROMETRIC, How to fulfill job experience, Pharma Industries and their job opportunities, How to survive in Pharma Industry, What is the growth in Pharma Industry. What is the features of Hospital Jobs. Here am giving introduction of Pharma category job and their importance. This is my Blogger agenda.

pharma guide is providing pharma job guidance and hospital pharmacy guidance. i am radhakrishna, am working as a pharmacist in kuwait.