LICQual Level 6 Diploma in Pharmaceutical Sciences (D Pharmaceutical Sciences) 

The LICQual Level 6 Diploma in Pharmaceutical Sciences (D Pharmaceutical Sciences) is a prestigious qualification designed for professionals seeking to advance their careers within the pharmaceutical industry. This comprehensive programme equips learners with an in-depth understanding of pharmaceutical sciences, including drug development, regulatory frameworks, clinical applications, and advanced research methodologies. By completing this diploma, learners can significantly enhance their expertise, broaden their professional horizons, and achieve valuable Continuing Professional Development (CPD) recognition.

This Level 6 Diploma is particularly suited to those working in pharmaceutical manufacturing, research and development, clinical trials, regulatory affairs, or related healthcare sectors. The curriculum is structured to foster critical thinking, problem-solving, and practical application of theoretical knowledge, ensuring learners are prepared for leadership and specialist roles.

To maintain the highest standards of learning, centres delivering this qualification must employ competent and qualified staff, and provide all necessary resources and materials. This commitment ensures a high-quality learning environment, enabling learners to gain the practical skills and academic knowledge required for success. Centres are also expected to support learners throughout their journey, offering guidance, feedback, and access to cutting-edge industry resources.

With a focus on excellence, professionalism, and career progression, the LICQual Level 6 Diploma in Pharmaceutical Sciences is the ideal choice for learners looking to elevate their skills, gain recognition within the industry, and achieve meaningful professional growth.

Course Overview


Qualification Title

LICQual Level 6 Diploma in Pharmaceutical Sciences (D Pharmaceutical Sciences) 

Total Units

6

Total Credits

120

GLH

480

Qualification #

LICQ2201191


Qualification Specification

Download Qualification Specification

To enroll in the LICQual Level 6 Diploma in Pharmaceutical Sciences (D Pharmaceutical Sciences) , applicants must meet the following criteria:

  • Age Requirement: Applicants must be at least 18 years old.
  • Educational Requirements: A Level 5 or Level 6 qualification in a relevant subject such as pharmaceutical sciences, chemistry, biology, or healthcare is required. Equivalent professional experience may also be considered.
  • Experience: Learners should have practical experience in the pharmaceutical or healthcare sector, demonstrating familiarity with industry practices, laboratory procedures, or clinical settings.
  • English Language Proficiency: Learners must have a strong command of English, both written and spoken, as all materials, assessments, and communications will be in English.
  • Commitment to CPD: Learners should demonstrate a strong commitment to Continuing Professional Development (CPD), as this qualification is designed to enhance professional knowledge, skills, and career progression.
  • Access to Required Resources: Learners must have access to the necessary learning materials, laboratories, and technological resources to complete practical and theoretical components successfully. Centres delivering the course must ensure all resources are available and fit for purpose.

Qualification#

Unit Title

Credits

GLH

LICQ2201191-1

Advanced Pharmaceutical Chemistry

20

80

LICQ2201191-2

Pharmacology and Therapeutics

20

80

LICQ2201191-3

Pharmaceutical Formulation and Drug Delivery

20

80

LICQ2201191-4

Regulatory Affairs and Quality Assurance

20

80

LICQ2201191-5

Clinical Research and Pharmacovigilance

20

80

LICQ2201191-6

Advanced Pharmaceutical Project

20

80

By the end of this course, learners will be able to:

Unit 1: Advanced Pharmaceutical Chemistry

By the end of this unit, learners will be able to:

  • Analyse organic, inorganic, and medicinal chemistry principles in pharmaceutical applications
  • Evaluate chemical reactions and mechanisms relevant to drug design and synthesis
  • Apply analytical techniques to solve complex problems in drug development
  • Critically assess the stability and formulation of chemical compounds for pharmaceutical use

Unit 2: Pharmacology and Therapeutics

By the end of this unit, learners will be able to:

  • Explain pharmacokinetics and pharmacodynamics and their impact on drug efficacy and safety
  • Analyse mechanisms of action and therapeutic applications of drugs
  • Evaluate modern treatment strategies and personalised medicine approaches
  • Apply pharmacological knowledge to support clinical decision-making and patient care

Unit 3: Pharmaceutical Formulation and Drug Delivery

By the end of this unit, learners will be able to:

  • Demonstrate understanding of advanced drug delivery systems, including controlled-release and targeted therapies
  • Analyse factors affecting drug absorption, distribution, metabolism, and excretion
  • Formulate pharmaceutical preparations according to scientific and regulatory guidelines
  • Critically evaluate innovative delivery technologies such as nanotechnology-based systems

Unit 4: Regulatory Affairs and Quality Assurance

By the end of this unit, learners will be able to:

  • Interpret national and international pharmaceutical regulations, including GMP and ISO standards
  • Develop quality management strategies for pharmaceutical production
  • Assess compliance and risk management processes in pharmaceutical environments
  • Apply regulatory knowledge to ensure safe and effective pharmaceutical practices

Unit 5: Clinical Research and Pharmacovigilance

By the end of this unit, learners will be able to:

  • Design and evaluate clinical trials following ethical and regulatory requirements
  • Analyse clinical data for safety, efficacy, and reliability
  • Implement pharmacovigilance processes to monitor adverse drug reactions
  • Apply evidence-based methods to improve drug development and patient outcomes

Unit 6: Advanced Pharmaceutical Project

By the end of this unit, learners will be able to:

  • Plan and execute an independent research project in a pharmaceutical context
  • Critically evaluate scientific literature and data relevant to the project topic
  • Demonstrate advanced analytical, problem-solving, and reporting skills
  • Present findings in a professional manner suitable for industry or academic settings

The LICQual Level 6 Diploma in Pharmaceutical Sciences is designed for learners who are looking to advance their careers and expertise in the pharmaceutical industry. This course is ideal for:

  • Pharmaceutical professionals aiming to enhance their knowledge of drug development, formulation, and regulatory practices.
  • Healthcare practitioners seeking to deepen their understanding of pharmacology, therapeutics, and clinical applications.
  • Research scientists and laboratory personnel interested in advanced pharmaceutical chemistry and innovative drug delivery systems.
  • Professionals in regulatory affairs and quality assurance who want to develop expertise in compliance, Good Manufacturing Practice (GMP), and risk management.
  • Learners aspiring to leadership or specialist roles within pharmaceutical manufacturing, clinical trials, or research and development.
  • Individuals committed to Continuing Professional Development (CPD) who wish to achieve industry-recognised qualifications and improve career prospects.
  • International professionals seeking a qualification aligned with UK and global pharmaceutical standards.

This course is tailored to professionals and learners who want practical, evidence-based knowledge combined with critical analytical skills to excel in the modern pharmaceutical sector.

To deliver the LICQual Level 6 Diploma in Pharmaceutical Sciences, centres must meet stringent standards to ensure high-quality training and learner success. Centres are expected to:

  • Employ competent and qualified staff with relevant academic qualifications and professional experience in pharmaceutical sciences, clinical research, or regulatory affairs.
  • Provide access to up-to-date learning materials and resources, including textbooks, scientific journals, laboratory equipment, and online platforms for theory and practical learning.
  • Maintain appropriate facilities and laboratories that meet health, safety, and industry standards for practical pharmaceutical training.
  • Implement robust assessment and feedback processes to support learner progression and ensure achievement of learning outcomes.
  • Ensure learners have access to digital resources and technology, including simulation tools, research databases, and software relevant to pharmaceutical practice and research.
  • Promote a culture of Continuing Professional Development (CPD), encouraging staff and learners to stay updated with industry advancements, new regulations, and scientific innovations.
  • Comply with national and international quality standards, including Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), and relevant regulatory frameworks.

By meeting these requirements, centres provide a high-quality learning environment, equipping learners with the knowledge, skills, and practical experience needed to succeed in the pharmaceutical industry.

Assessment and Verification

All units within this qualification are subject to internal assessment by the approved centre and external verification by LICQual. The qualification follows a criterion-referenced assessment approach, ensuring that learners meet all specified learning outcomes.

To achieve a ‘Pass’ in any unit, learners must provide valid, sufficient, and authentic evidence demonstrating their attainment of all learning outcomes and compliance with the prescribed assessment criteria. The Assessor is responsible for evaluating the evidence and determining whether the learner has successfully met the required standards.

Assessors must maintain a clear and comprehensive audit trail, documenting the basis for their assessment decisions to ensure transparency, consistency, and compliance with quality assurance requirements.

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