Create Change in Your Life - Realize Your Vision

Vision is a big part of that and there is a big difference in vision and sight. Let me make a distinction here. Sight is seeing with the eyes. Vision is seeing through the eyes.


Let’s talk about vision. That’s a big, big piece of being able to create to create what you choose to create in your life. Be able to create magic, literally. I define magic as the ability to create willful change in a fabric of your universe, both spiritually and materially. Vision is a big part of that and there is a big difference in vision and sight. Let me make a distinction here. Sight is seeing with the eyes. Vision is seeing through the eyes. I guarantee you this, when the vision on the inside becomes more compelling and powerful than what you observe on the outside, and then the universe is at your command. It really is.

Most people live their life as sight. A dog can do that. Animals can live by their sensory factors. You are more than that. What we must do is rise above our sensory factors and create that vision internally that modern science now tells us is then projected outward in the world. That is just not medical/physical foo foo anymore. That is reality. We literally project our world outside of us from the vision we have internally.

The ability to create willful change is what vision is all about. My friend James Ray calls that magic. Magic isn’t rabbits being pulled out of hats. It is ability to create willful change in the fabric of your universe, both spiritually and materially. Vision is a big part of that magic. Unless you have a strong imagination, and just look at the word imagination, image is a big part of that word.

If you don’t have the ability to image internally and to envision internally what you choose to create, then you are not going to be able to create that willful change. If you do, the universe is at your command. You are going to have to be able to turn away from sight or the sensory factors, which is seeing with the eyes vs. seeing through the eyes.

I experience it as something that a visionary feeling you have inside you. You can see it, you can feel it. You kind of immerse yourself in the concept of what you want to be.

If you look at the word motion, 99% of that work is motion. If you look at the work motivation, 2/3 of the word motivation is motion. Motion and emotion create vibrations within our body which are the feelings and vibrational universe that is the message you are sending out to the universe and going to attract the law of attraction. Being the law of attracting, those feelings of visual vibrations are going to attract into your life what you are in alignment with. You are never, ever, ever going to attract diamonds into your life if you are resonating with rocks.

Scott Martineau

Quick Short Term Cash Loan – Easy Money for All Your Needs

Quick short term cash loans are ideal for everyone. It can be availed by both tenants and homeowners. It can be used for vacation; wedding, paying debts etc. quick cash short term loans are available both through online market and thorough physical lenders.


Sometimes it becomes necessary to generate extra cash for fulfilling urgent needs. Quick short term cash loan is the best way to do so. Short term cash loans are meant for people in urgent need of monetary assistance.

Information

Short term cash loans are available in the market in both secured and unsecured forms. Secured cash loans can be availed by placing a property as collateral with the lender. This can be any personal property like home, car, bank balance etc. on the other hand unsecured short term loans can be availed without placing any such security against the loan amount. Short term cash loans are open to both good credit borrowers and bad credit borrowers. People suffering from arrears, defaults, CCJ’s, IVA etc are eligible to avail cash loans. Bad creditors can increase their chances of loan approval by opting for secured quick cash loans.

Amount and Interest

Amount that can be borrowed varies from lender to lender. In general the amount that can be availed with short term cash loans ranges from £ 1000 - £ 25000. The loan amount depends upon the credit status, repayment ability and bank details of the borrower. Repayment duration of quick short term cash loan is quite flexible that ranges from 1- 10 years. Quick short term cash loan carries higher interest rate compared to other loans because it is short term in nature but there are many through it can be brought down. The best way to lower the interest rate is applying for secured quick short term cash loan. Deep search of the financial market is advisable in order to lower the interest rate if you don’t have any personal property or if you don’t want to risk your property.

Usage

You can use short term loans for any of your needs. You can use it to renovate your home, vacation, wedding and so on. Also, you can use it to pay urgent bills, loan instalments, debts etc.

Application

Applying for short term loans is very easy. To apply all you need to do is fill up an application form providing information like your address, phone number, employer etc either by visiting a lender or through online method.

Shain Johnson

Essential Elements Of Quality Management System

Essential elements of a good quality management system are described in this article for pharmaceutical industry.

A good quality management system in a pharmaceutical company can significantly improve the net profit status, high quality medicines for patients, less rework and recall which save more money, good work environment and compliance with local and international regulations.



Quality management is a philosophy. It takes management understanding, commitment and responsibility before introducing and implementing the concept. Once practiced a good quality management system slowly develop or reshape a sustainable organization culture that pays off rapidly.

The initial step of introducing a good quality management into a system is to know the essential elements of the quality system and clear study from where to start. Company objectives should be clearly understood. Policies should be prepared. Then comes the design of the process flow, validating the process, material flow and organization chart. When a good integration between people, process and material is achieved the next step is to putting the integrated system in a state of control. Any deviation from the controlled system must be analyzed and corrected.

Some basic but essential elements of Quality Assurance as depicted in GMP guidelines and ISO 9001 guideline for pharmaceutical industry can be listed as: the Preparation of standard operating procedures of a complete system maintaining cGMP principles; Preparation and maintenance of effective change control of quality and master file documentation; Recording and management of manufacturing change control; Recording and reporting procedure of Deviations of your systems; Quality concern investigation process; Customer complaint investigation procedure; Quality audit procedures; Vendor assessment, evaluation and certification procedure; Quality control laboratory procedure, Rework procedures for the defective manufactured products; Procedures on training for manufacturing staffs and recall procedure.

Standard operating procedures and manuals should be written in details and referenced to relevant other documents, so a new starter within the organization should be trained easily and expected to perform as per procedure. The result will be a common standard of activities across the organization, good tractability of work flow, deviations and ease of corrective actions as necessary.

Standard Operating Procedure

You should prepare SOPs, forms, templates and manuals, which can be used immediately as the system runs. Forms and templates should be used for record keeping which your people can follow routinely.

Documentations - Classification, Definition and Approval

Quality and Technical/Master file documents to be created to build up a good quality management system for your manufacturing sites. Definition of documents, their classification, approval requirements and retention requirements should be understood.

Quality Documentation Management and Change Control

Procedures to be created on how to generate new quality documents or change control of existing documents, review of quality documents, satellite file management, role of document author, approver, document control officer and satellite file administrator. In this procedures you will also define the numbering systems of different quality documents like audit files, SOPs, forms, templates, manuals, training files, QA agreements, project files etc and their effective archiving system.

Preparation, Maintenance and Change Control of Master Documents

Procedures to be created which will particularly focus on the management of master file documents like specifications, control methods, raw materials, finished goods and packaging specification and test reports, formulation, stability files etc required to generate during the product registration in the market.

Deviation Report System

It is a regulatory requirement to capture all sorts of deviations evolves in your systems in order to maintain the continuous improvement of your processes and systems. Procedures should be created that describes how to categorize the deviations between production, audit, quality improvements, technical deviations, customer complaints and environmental, health and safety deviations. It should also describes the management responsibilities of initiating deviation, capturing data, analysis, investigation, determination of assignable cause/s, generation of management report and initiatives to be taken on corrective and preventative actions.

Vendor Selection and Evaluation

Procedures to be followed during the vendor assessment and vendor evaluation for purchasing of raw materials, critical and non critical packaging components, laboratory supplies, engineering supplies and imported finished goods from the vendor. These instructions are essential for approving prospective vendor.

Vendor Certification

This procedure aims to describe the process by which a vendor may be certified to supply materials or services. This procedure applies to vendors that supply a material or service to be used at any stage of manufacture by operations. Here you will describe the roles of each department in the process to certify an approved vendor.

Product Complaint Procedure

You should have strong procedure to cover the receipt, logging, evaluation, investigation and reporting system of all complaints received from customers for the marketed products. This procedure should contain step by step instruction to be followed during the customer complaint management like numbering of complaint, registering the complaint, evaluation, determination of assignable cause for the complaint deviation, implementation of corrective and preventative actions, trending of complaints and handling of counterfeit products.

Annual Product Review

Some countries require reports as Annual Product Review to sell your products into their market. So you have to create instructions on how to do annual product review, to evaluate data, trends and to identify any preventative or corrective action that would lead to product quality improvements and report them to management.

Rework Procedure

Procedure should contain the step by step instructions to be followed when the rework of an in-process or completed finished good is required.

Product Identification and Traceability

The purpose of this procedure is to define the method used for the identification of all contributing materials that could affect product quality and to ensure their full traceability.

GMP Audits

Procedure should be created to describe the process of planning, performing, reporting and follow-up of different audits for your systems like Internal Quality audit, Vendor audit, Environmental Health and Safety (EHS) audit, EHS workplace inspection, Housekeeping audit.

Evaluation of Batch Documentation and Release for Sale

This procedure should describe the process of collection, evaluation and record of batch related document generated during the production of a batch before an authorized person can release the batch for sale.

GMP Training

Effective GMP related training modules to be created for your manufacturing staffs. Training records and reports have to produce on each employee as justified.

Management and Control of Contract Work

There should have procedure to describe the management and control of contract work provided by the contractors for packaging and finished products for your company as well as control of contract works done by your company on behalf of others.

Quality Concern Investigation Process

Procedure should be made that contains instructions to follow when conducting Investigations collection of data and information, analysis, assigning root cause, determine corrective and preventive actions.

Sami