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NDA to PLC terms

The List of Abbreviations used in Pharmaceutical Industry

Check out more information of related terms

In Chapter Eight of the list of abbreviations used in pharmaceutical Industry there are some terms used in research and development activities related to pharma industry.

  1. NDA: New Drug Application
  2. NF: National Formulary
  3. NIR: Near Infra Red Spectroscopy
  4. NON: Notice of non-compliance (Canada)
  5. ODI: Orally Disintegrating Tablet
  6. OQ: Operation Qualification
  7. OSD: Oral Solid Dosage
  8. OSHA: Occupational Safety And Health Administration
  9. OTC: Over-the-counter
  10. OOS: Out of specification
  11. OOT: Out of trend
  12. PAC: Post-approval changes
  13. PAO: Poly alpha olefin
  14. PAT: Process Analytical technology
  15. PET: Preservative efficacy test
  16. PET: Polyethylene
  17. PIC/S: Pharmaceutical Inspection Co-operation Scheme
  18. PLC: Programmable Logic Control

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  • The List of Abbreviations used in Pharmaceutical Industry

    You've already read about various topics related to Pharma Industry.Well, today I want to introduce you to the List of Abbreviations used in Pharmaceutical Industry.

    There are lots of topics related to pharmacy which are available on the internet. We have studied a lot about various activities carried out daily in pharma industry so it is very important to know all the terms used in pharma.

    Here is what you are goint learn in the List of Abreviations used in Pharmaceutical Industry:

  • ICAH to LDPE terms

    The List of Abbreviations used in Pharmaceutical Industry

    Check out more information of related terms

    Get some more about the list of abbreviations used in pharmaceutical industry in chapter Six. Following are some of the ueful terms which are used in pharma industry.

  • SOP to WL terms

    The List of Abbreviations used in Pharmaceutical Industry

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    The last chapter of the list of abbreviations used in pharmaceutical industry is chapter number ten. Other important meaning and terms are given here. so check out all the terms one by one.

  • CFR to EIR terms

    The List of Abbreviations used in Pharmaceutical Industry

    Check out useful information on related terms.

    The third chapter of the List of abbreviations used in pharmaceutical Industry is as follows so let us know some of the terms used in pharma.

  • PQ to SMF terms

    The List of Abbreviations used in Pharmaceutical Industry

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    In Chapter number nine of the list of abbreviations used in pharmaceutical Industry you will get some of the other words used in pharma industry which are given below.

  • Introduction

    The List of Abbreviations used in Pharmaceutical Industry

    Check out more information of related terms

    We wanted to give you thehe most extensive and detailed list of useful abbreviations in pharmaceutical industry that exists today

    If you’ve only read about Pharmaceutical Industry, if you want to learn more about some of the important information of pharma industry, then this List of Abbreviations Used in Pharmaceutical Industry is for you.

  • LIMS to NCE terms

    The List of Abbreviations used in Pharmaceutical Industry

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    Again in the seventh chapter of the list of abbreviations used in pharmaceutical industry you will get some of the important terms used daily in pharma industry.

  • EMEA to GC terms

    The List of Abbreviations used in Pharmaceutical Industry

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    The fourth chapter of the list of abbreviations used in pharmaceutical industry also contains some of the useful terms so check out one by one which are given as follows.

  • BET to CEP terms

    The list of Abbreviations used in Pharmaceutical Industry

    Check out useful information on related terms.

    In the Second Chapter on List of abbreviations used in pharmaceutical Industry find out more informations of the useful terms. Some of them are given below so check it out one by one.

  • AADA to BCS terms

    The list of Abbreviations used in Pharmaceutical Industry

    Check out more information on related terms.

    Welcome to the first chapter on the List of Abbreviations used in Pharmaceutical Industry. All the terms used in pharma are given below so check it out one by one.

  • GCLP to HVAC terms

    The List of Abbreviations used in Pharmaceutical Industry

    Check out more information of related terms

    In the fifth chapter of the list of abbreviations used in pharmaceutical industry know some more meaning of useful terms. They are given below so find out one by one.

  • Process Validation Stages process qualification report excution

    In Process Validation the execution of process qualification begins after the approval of the protocol, Following are some of the points regarding execution and preparation of report during process qualification.

    Execution will start of begins after the approval of the protocol.

    All points mentioned in the protocol are to be followed.

    If the points mentioned in protocol is not followed then proper justification is required.

    Follow the commercial manufacturing process and the routine procedures.

  • Process Validation Stages process qualification one

    In Process Validation the second stage that is process qualification , the design of the facilities and the qualification of the equipment and the qualification of the utilities are very important. Some of the points regarding design and qualification are as follows:

    During the qualification of th utilities and the equipment, the construction materials, the operating principle and the performance characteristics are very important.

  • Process Validation Stages process qualification protocol

    During Process Validation the protocol of process qualification is also prepared, following are some of the points which are included into protocol of process qualification, so let us check it out some points:

    The manufacturing condition including processing limits, the operating parameters as well as the components used such as raw materials are included in protocol.

    The sampling plan with complete details of the number of sampling points, frequency of sampling of each unit are to be mentioned in protocol.

  • Process Validation Stages process qualification

    During Process validation: The second stage is process qualification Some of the points which are discussed during process qualification are as follows , so let us check it out points one by one.:

    The main aim of process qualification is to determine whether the process which is designed is capable of reproducible commercial manufacture or not.

    Design of the utility and the qualification of the equipment are taken into account during process qualification.

    Process performance qualification in this stage.

  • Process Validation Stages process qualification two

    In the Process Validation during second stage that is process qualification some more points are taken into account which are  discussed below. So let us see some points one by one:

    During process performance qualification the actual facilities, utilities and equipment are checked whether they are qualified or not.

    The personnel operating various equipment are trained or not is checked.

    The  procedure which are performed are as per standard procedure is verified and checked.

  • Importance of Sustainable Development in Points

    Check out Importance of Sustainable Development in Points which are discussed below. So let us find out some important points on importance to know more about sustainable development.

    Importance of sustainable developement are :

    Sustainable Development is a continuous Process

    Sustainable development helps in developing eco-friendly culture.

    Sustainable development considers the needs for future generation

    Freedom of speech and freedom of choice in sustainable development.

    Improves economic growth as well as national wealth.

  • What are "Tablet Coating - Defects"?

    List of  some tablet coating defects which may affect the tablet formulation and bioavailability of drug are as follows.

    (1) Picking and Sticking,

    (2) Color variation,

    (3) Orange peel effect,

    (4) Twinning,

    (5) Capping and lamination,

    (6) Mottled color,

    (7) Roughness,

    (8) Hazing or Dull film

    (9) Bridging,

    (10) Erosion,

    (11) Filling,

    (12) Chipping,

    (13) Blistering,

    (14) Cracking,

    (15)  Peeling and frosting.

  • Advantages and disadvantages of solid phase extraction

    Solid phase extraction:Let us discuss advantages and disadvantages of solid phase extraction. Some of them are discussed below so let us check it out one by one.

    Advantages:

    No emulsion problems observed.

    Cost is low

    Accuracy is greater

    Glass breakage minimal

    Lower solvent consumption

    Reagent consumption lower

    No cross contamination

    Less sample handling

    Process in fewer steps

    Disadvantages:

    Incomplete removal of the interferences

  • Process Validation Stages process design two

    In Process validation the first stage that is Process design stage have some points which are taken into account. Some of them which are taken into consideration are as follows:

    Process control should address variability such as:

    During the process design the control to reduce the input variation and the control to adjust for input variation are taken into account during manufacturing.

    Controls may also consist of about the equipment monitoring at significant processing point and also control on material analysis.

  • Process Validation Stages

    Process Validation is divided into three stages, So let us check it out one by one. Following are the three stages.

    Stage I - Process Design: With the knowledge of Scale up studies and the prior knowledge which is gained through development, The commercial manufacturing process is defined during this stage of process design.

    Stage II - Process Qualification: After defining process design, it is evaluated in this stage to determine whether the process is capable of reproducible commercial manufacturing or not.

  • Process Validation Types Prospective validation

    Types of Process validation:Out of four types prospective validation is one of them. Some points regarding prospective validation are as follows , so let us check it out one by one:

    In prospective validation process the validation is carried out based on the pre planned protocols.

    Prospective validation is carried out at new process at new manufacturing facility.

    Before pharmaceutical production at commercial level, prospective validation is carried out.

    During prospective validation the input resources are clearly defined and specified.

  • Process Validation stages continued process verification one

    About Process Validation, the third stage is continued process verification, Some more information about process validation in continued process verification are as follows:

    The variation in the continued process verification can be detected by assessment of various documents.

    By complaints of any defects.

    By checking out of specification records or process parameters.

    Checking deviation reports.

    By observing variation in the process yield.

    By checking batch records.

    Checking records of incoming materials.

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Metals Recycling

Recycling of metals such as copper, aluminium etc., is required to protect earth and environment. It also saves energy and natural resources. Along with benefits there are some drawbacks of recycling metals. 

Full Form of UPA and NDA

Full Form of UPA and NDA are as follows , so let us check it out some information on UPA and NDA to know more about it.

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How is Coal Formed ?

Since the 13th century coal is derived from the Old English term col, which means "mineral of fossilized carbon".

Coal consists of high content of carbon and other elements like, sulfur, hydrogen, oxygen, and nitrogen.

Coal is a naturally black sedimentary rock occurring in rock strata in layers or veins called coal beds or coal seams.

Anthracite coal is the solider form of coal, can be considered as metamorphic rock because of later exposure to high temperature and pressure.